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  • Dispositivo 500
  • Fabricante 31827
  • Evento 523
  • Implante 1
Device Recall Unloader XT
  • Modelo / Serial
    Item No: B-102500010 B-102500020 B-102600010 B-102600020
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    U.S. distribution to the following; AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
  • Descripción del producto
    Unloader XT || Product Usage: || Unloader XT Extreme is an external knee braces to provide support for knee instability due to ligament injuries and osteoarthritis.
  • Manufacturer
    Ossur H / F
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Unloader XT
Device Recall Unloader Custom Lite
  • Modelo / Serial
    Item No: B-107500020 B-107600020
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    U.S. distribution to the following; AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
  • Descripción del producto
    Unloader Custom Lite || Product Usage: || Unloader Custom Lite is an external knee braces to provide support for knee instability due to ligament injuries and osteoarthritis.
  • Manufacturer
    Ossur H / F
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Unloader Custom Lite
Device Recall Unloader Custom
  • Modelo / Serial
    Item No: B-122500020 B-122600020
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    U.S. distribution to the following; AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
  • Descripción del producto
    Unloader Custom || Product Usage: || Unloader Custom is an external knee braces to provide support for knee instability due to ligament injuries and osteoarthritis.
  • Manufacturer
    Ossur H / F
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Unloader Custom
Device Recall Extreme Custom
  • Modelo / Serial
    Item No: B-108500010 B-108500020 B-108600010 B-108600020 B-123500020 B-123600020
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    U.S. distribution to the following; AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
  • Descripción del producto
    Extreme Custom || Product Usage: || Extreme Custom is an external knee braces to provide support for knee instability due to ligament injuries and osteoarthritis.
  • Manufacturer
    Ossur H / F
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Extreme Custom
Device Recall Papoose Infant Spine Immobilizer, Papoose; Papoose w/replacement pads; Papoose w/o...
  • Modelo / Serial
    Item # Item Description: PA-100 Papoose PAR-100 Papoose w/replacement pads PO-100 Papoose w/o PO front POR-100 Papoose w/o PO front w/pad   All lot numbers from MX140101 to MX150930
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    U.S. distribution to the following; AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
  • Descripción del producto
    Papoose Infant Spine Immobilizer || Item # Item Description: || PA-100 Papoose || PAR-100 Papoose w/replacement pads || PO-100 Papoose w/o PO front || POR-100 Papoose w/o PO front w/pad || Product Usage: || The Papoose Infant Immobilizer is an external class I orthotic device used to securely immobilize the head and spine in the proper anatomical airway and spinal alignment. The occipital shape protects against positional plagiocephaly.
  • Manufacturer
    Ossur H / F
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Papoose Infant Spine Immobilizer, Papoose; Papoose w/replacement pads; Papoose w/o PO front;'/ pad
Device Recall Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom)
  • Modelo / Serial
    The hydraulic jack assemblies (Part numbers: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) used as service parts on Stretchers assembled from 8/28/15 - 8/29/15
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed in DC and the states of AL, CA, FL, MN, MT, NC, NE, NY, PA, RI, TN, TX, UT, and WV.
  • Descripción del producto
    Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) || Powered stretcher
  • Manufacturer
    Stryker Medical Division of Stryker Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom)
Device Recall Acorn Stairlifts
  • Modelo / Serial
    Serial Numbers: 140401487591 to 140410249946. All models manufactured before April 2012
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA (nationwide) Distribution to the states of : AL, AZ, CA, CO, DE, FL, GA, IL, IN, KS, KY, LA, MA, ME, MD, MI, MO, NH, NJ, NY, NC, OH, PA, RI, SC, TN, TX, UT, VT, VI, WA, WV, WI, and District of Columbia and to the countries of UK and Germany.
  • Descripción del producto
    Acorn 180 Curved Stairlift
  • Manufacturer
    Acorn Stairlifts Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Acorn Stairlifts
Device Recall AdTech Electrode Connection System/Cables
  • Modelo / Serial
    Lot Numbers: 208140507, 208140552, 208140556, 208140559, 208140560, 208140561, 208140562, 208140563, 208140564R, 208140579, 208140581, 208140586, 208140588R, 208140590, 208140604.
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed in the states of GA and MI, and the countries of FRANCE, UNITED KINGDOM, COLOMBIA, and BRAZIL.
  • Descripción del producto
    Ad-Tech Electrode Connection System/Cables. Lightweight TECH-ATTACH Cable Models: || 1. L-DCL-4DINX (4 contacts: 1 terminal block with 4 connectors each); || 2. L-DCL-6DINX (6 contacts: 1 terminal block with 6 connectors each); || 3. L-DCL-8DINX (8 contacts: 1 terminal block with 8 connectors each); || 4. L-DCL-16BDINX (16 contacts: 1 terminal block with 16 connectors each); || 5. L-DCL-32BDINX (32 contacts: 2 terminal blocks with 16 connectors each); || 6. L-DCL-64BDINX (64 contacts: 4 terminal blocks with 16 connectors each). || FO TECH-ATTACH Connection Cable model FO-LDC-4DINX (4 contacts: 1 terminal block with 4 connectors each). || Tech-Attach: these cables require the use of an additional component - the connector block. The tail of the electrode is inserted into the block and the block in turn mates with the cable. A key-pin is used to ensure proper orientation. The cable terminated in EEG compatible connector sockets. || Lightweight CABRIO Cable, model L-SRL-64BDINX (64 contacts: 4 terminal blocks with 16 connectors each). Cabrio cables are similar to Tech-Attach cables except that the block portion is pre-attached. The tail of an electrode is inserted into this portion which then hinges shut.
  • Manufacturer
    Ad-Tech Medical Instrument Corporation
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall AdTech Electrode Connection System/Cables
Device Recall reVive Light Therapy Pain Relief Device
  • Modelo / Serial
    Manufactured between 12/15/2015 and 12/28/2015 for specific lot #1052
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed to 1 consignee located in the United States.
  • Descripción del producto
    reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) || Product Usage: || The reVive Light Therapy Pain Relief Device is a device designed to deliver LED light spectrum in 880nm and 660nm directly into the body tissue to increase circulation and temporarily relieve pain associated with muscle spasms, arthritis, general aches and strains.
  • Manufacturer
    LED Technologies, LLC
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall reVive Light Therapy Pain Relief Device
Device Recall Aluminum crutch
  • Modelo / Serial
    Item #.: 1) 10400-1, 2) 10400-8, 3) 10401-1, 4) 10401-8, 5) 10402-1 & 6) 10402-8
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Aluminum crutch under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, adult, 8 pairs per case, 3) Aluminum crutch, youth, 1 pair per case, 4) Aluminum crutch 8 pairs per case, 5) Aluminum crutch, tall adult, 1 pair per case & 6) Aluminum crutch, tall adult, 8 pairs per case
  • Manufacturer
    Medical Depot Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Aluminum crutch
Device Recall EZ adjust aluminum crutch
  • Modelo / Serial
    Item #: 1) 10430-1, 2) 10430-8, 3) 10431-1, 4) 10431-8, 5) 10432-1 & 6) 10432-8
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ adjust aluminum crutch, tall adult, 1 pair per case & 6) EZ adjust aluminum crutch, tall adult, 8 pairs per case
  • Manufacturer
    Medical Depot Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall EZ adjust aluminum crutch
Device Recall Universal aluminum crutch
  • Modelo / Serial
    Item #: RTL 10433
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Universal aluminum crutch, 1 pair per case || Aid the user in walking while relieving weight from one foot or leg.
  • Manufacturer
    Medical Depot Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Universal aluminum crutch
Device Recall Universal Quick Adjust
  • Modelo / Serial
    Item #: 1) RTL 10400, 2) RTL 10402
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case || Aid the user in walking while relieving weight from one foot or leg.
  • Manufacturer
    Medical Depot Inc.
  • 2 Events
    • Retiro De Equipo (Recall) de Device Recall Universal Quick Adjust
    • Retiro De Equipo (Recall) de Device Recall Universal Quick Adjust
Device Recall Direct Supply aluminum crutch
  • Modelo / Serial
    Item #: DS 10400
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    Direct Supply aluminum crutch, adult, 1 pair per case || Aid the user in walking while relieving weight from one foot or leg.
  • Manufacturer
    Medical Depot Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Direct Supply aluminum crutch
Device Recall HeaterBaum Foot & Ankle Heating Pad
  • Modelo / Serial
    All lots; UPC: 862821000030.
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- US, including the states of AL, AR, CA, FL, GA, KS, MA, MD, ME, MI, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, PA, TN, TX, UT, VA, and WA; and, the countries of Ecuador & Venezuela.
  • Descripción del producto
    HeaterBaum Foot & Ankle Heating Pad, Heating Soft Compression Therapeutic Boot with Precise Temperature Control Thermostat, 110 V with AC Adapter.
  • Manufacturer
    Ergoactives, Llc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall HeaterBaum Foot & Ankle Heating Pad
Device Recall Quickie Q7 wheelchair. Model EIR4
  • Modelo / Serial
    Model EIR 4 13,000 + serial numbers. RES would not accept this number. Please see spreadsheet provided in documents.R4-007239 to R4-022394. Serial number range:
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US and Mexico, Japan, Chile, Kuwait, Columbia, Hong Kong, China, Uruguay, South Africa, Costa Rica, South Korea, Singapore, New Zealand, El Salvador, Bahrain, Uruguay, Lebanon, United Arab Emirates, Brazil, Argentina, Netherlands Antilles, British Virgin Islands,
  • Descripción del producto
    Quickie Q7 wheelchair. Model EIR4 || Physical Medicine. || The Quickie Q7 series of wheelchair's intended use is to provide mobility to persons limited to a sitting position.
  • Manufacturer
    Sunrise Medical (US) LLC
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Quickie Q7 wheelchair. Model EIR4
Device Recall Journey Rolling Walker
  • Modelo / Serial
    Serial No. YA 4205RDFG004 TO YA4205RDFG0098 YZ4205BKFC0002 TO YZ4205RDFE0100
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution in the states of: CA, IN, HI, CT, UT, WA, FL, VA, WI, OH, MN, KS, MD, IL, MO, WY, MT, ME, PA, TN, MI, OR, NY, NJ, ID, NC, IA, OK, AR, VT, SC, TX
  • Descripción del producto
    4205 Journey Rolling Walker || Product Usage: used to assist people in walking
  • Manufacturer
    Nova Ortho-Med Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Journey Rolling Walker
Device Recall TENNIS ELBOW SUPPORT
  • Modelo / Serial
    Lots: 42249787, 42490802, 42737908, 42944296, 43000801, 43031421, 43036118, 43068890, 43134851, 4363109, and 43454441
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution
  • Descripción del producto
    TENNIS ELBOW SUPPORT, PneuGel(TM), UNIVERSAL, REF 200A10, QTY: 1 Each, Rx Only, || Product Usage: || Lateral and medial epicondylitis
  • Manufacturer
    DeRoyal Industries Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall TENNIS ELBOW SUPPORT
Device Recall TENNIS ELBOW SUPPORT
  • Modelo / Serial
    Lots: 47001, 49894, and 51311
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution
  • Descripción del producto
    PNEUGEL(R) TENNIS ELBOW STRAP, UNIVERSAL, REF 12840000, QTY: 1 Each, Rx Only, || Product Usage: || Lateral and medial epicondylitis
  • Manufacturer
    DeRoyal Industries Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall TENNIS ELBOW SUPPORT
Device Recall TRUBalance3 Power Positioning System
  • Modelo / Serial
    Numerous serial numbers affected (12,343 units)
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). || Mobility Medical Device
  • Manufacturer
    Pride Mobility Products Corp
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall TRUBalance3 Power Positioning System
Device Recall Arial WaterResistant Pendant, model 59350
  • Modelo / Serial
    Serial numbers WP149149 through WP149398 and WP149649 through WP149898.
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution to AR, AZ, CA, FL, GA, IA, ID, IN, KS, MD, MN, MO, NC, NE, NJ, NY, OH, OR, PA, SD, UT, VA, and WI.
  • Descripción del producto
    Arial Wireless Water-Resistant Call Pendant || The Arial Pendant tag is part of the Arial wireless emergency call management system. It enables residents in assisted living, skilled nursing or independent living to call staff with the press of a button.
  • Manufacturer
    Stanley Security Solutions Inc
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Arial WaterResistant Pendant, model 59350
Device Recall Hidrex USA DP450
  • Modelo / Serial
    SN# 16-3.7091 to 16-3.7134, 17-3.7001 to 17-3.7020
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide throughout the US
  • Descripción del producto
    Hidrex USA DP450
  • Manufacturer
    Hidrex GmbH
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Hidrex USA DP450
Device Recall Hidrex USA DVP1000
  • Modelo / Serial
    SN# 16-3.6190 to 16-3.6319, 17-3.6001 to 17-3.6050
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide throughout the US
  • Descripción del producto
    Hidrex USA DVP1000
  • Manufacturer
    Hidrex GmbH
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Hidrex USA DVP1000
Device Recall Daavlin Aquex (DAAV1000)
  • Modelo / Serial
    SN# 16-3.8001 to 16-3.8250
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide throughout the US
  • Descripción del producto
    Daavlin Aquex (DAAV1000)
  • Manufacturer
    Hidrex GmbH
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall Daavlin Aquex (DAAV1000)
Device Recall ROHO HIGH PROFILE Single Compartment Cushion
  • Modelo / Serial
    Serial Numbers: A2920163 through A3185287 Model Numbers: 1R1010H-CA-SC, 1R109M-CA-SR, 1R1211H-CH-SR, 1R88H-CA-SR, 1R1010H-CA-SCDM, 1R109M-CF-SR, 1R1212H-CA-SR, 1R88H-CF-SR, 1R1010H-CA-SR, 1R109M-CH-SR, 1R1212H-CH-SR, 1R88H-CH-SR, 1R1010H-CF-SCDM, 1R1110H-CA-SC, 1R129H-CA-SR, 1R88M-CA-SR, 1R1010H-CF-SR, 1R1110H-CA-SR, 1R1310H-CA-SR, 1R88M-CF-SR, 1R1010H-CH-SR, 1R1110H-CF-SR, 1R1310H-CF-SR, 1R89H-CA-SR, 1R1010M-CA-SC, 1R1110H-CH-SC, 1R1311H-CA-SR, 1R89H-CF-SR, 1R1010M-CA-SCDM, 1R1110H-CH-SR, 1R1311H-CH-SR, 1R89M-CA-SR, 1R1010M-CA-SR, 1R1110M-CA-SR, 1R1411H-CA-SR, 1R89M-CF-SR, 1R1010M-CF-SCDM, 1R1110M-CF-SR, 1R1411H-CF-SR, 1R910H-CA-SR, 1R1010M-CF-SR, 1R1110M-CH-SC, 1R1511H-CA-SR, 1R910H-CF-SR, 1R1010M-CH-SR, 1R1110M-CH-SR, 1R66H-CA-SR, 1R910H-CH-SC, 1R1011H-CA-SC, 1R1111H-CA-SC, 1R66H-CF-SR, 1R910H-CH-SR, 1R1011H-CA-SR, 1R1111H-CA-SR, 1R67H-CF-SR, 1R910M-CA-SR, 1R1011H-CF-SR, 1R1111H-CF-SR, 1R77H-CA-SR, 1R910M-CF-SR, 1R1011H-CH-SC, 1R1111H-CH-SC, 1R77H-CF-SR, 1R911H-CA-SC, 1R1011H-CH-SR, 1R1111H-CH-SR, 1R77M-CA-SR, 1R911H-CA-SR, 1R1011M-CA-SC, 1R1111M-CA-SR, 1R77M-CF-SR, 1R911H-CF-SR, 1R1011M-CA-SR, 1R1111M-CF-SR, 1R78H-CA-SR, 1R911H-CH-SR, 1R1011M-CF-SR, 1R1111M-CH-SR, 1R78H-CF-SR, 1R98H-CA-SR, 1R1012H-CA-SR, 1R1112H-CA-SR, 1R78M-CA-SR, 1R98H-CF-SR, 1R1012H-CF-SR, 1R1112H-CF-SR, 1R78M-CF-SR, 1R99H-CA-SC, 1R1012H-CH-SR, 1R1112H-CH-SR, 1R79H-CA-SR, 1R99H-CA-SCDM, 1R108H-CA-SR, 1R119H-CA-SC, 1R79H-CF-SR, 1R99H-CA-SR, 1R108H-CF-SR, 1R119H-CA-SR, 1R810H-CA-SR, 1R99H-CF-SCDM, 1R109H-CA-SCDM, 1R119H-CF-SR, 1R810H-CF-SR, 1R99H-CF-SR, 1R109H-CA-SR, 1R1210H-CA-SC, 1R810M-CA-SR, 1R99H-CH-SR, 1R109H-CF-SCDM, 1R1210H-CA-SR, 1R87H-CA-SC, 1R99M-CA-SR, 1R109H-CF-SR, 1R1210H-CF-SR, 1R87H-CA-SR, 1R99M-CF-SR, 1R109H-CH-SC, 1R1210H-CH-SR, 1R87H-CF-SR, 1R99M-CH-SR, 1R109H-CH-SR, 1R1211H-CA-SR
  • Clasificación del producto
    Physical Medicine Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide, Sweden, Germany, New Zealand, Finland, Australia, Singapore, Korea, Luxembourg, Czech Republic, South Africa, Canada, Switzerland, United Arab Emirates, Spain, Austria, Hong Kong, Iceland, Japan, Canada, Italy, Ireland, France, United Kingdom
  • Descripción del producto
    ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology and ROHO MID PROFILE Single Compartment Cushion with Sensor Ready Technology.
  • Manufacturer
    Roho Inc.
  • 1 Event
    • Retiro De Equipo (Recall) de Device Recall ROHO HIGH PROFILE Single Compartment Cushion
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Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.