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  • Dispositivo 2073
  • Fabricante 2073
  • Evento 2209
  • Implante 0
Ventilator - E360E / E360S / E360S / E360S / E360T / E360T + - Anvisa Registration No. 8011301002...
  • Modelo / Serial
  • Manufacturer
    RESPIRATORY CARE HOSPITALAR LTDA.; Newport Medical Instruments
  • 1 Event
    • Alerta De Seguridad para Ventilator - E360E / E360S / E360S / E360S / E360T / E360T + - Anvisa Registration No. 80113010025 - Risk Class III ## Series Affected: See Distribution Map in Annex 1
Ventilator - E360BR - Anvisa Registration No. 80113010007 - Risk Class III ## Series Affected: E3...
  • Modelo / Serial
  • Manufacturer
    RESPIRATORY CARE HOSPITALAR LTDA.
  • 1 Event
    • Alerta De Seguridad para Ventilator - E360BR - Anvisa Registration No. 80113010007 - Risk Class III ## Series Affected: E360A1011188 to E360A1211170 / E360TA0113013 to E360TA1213066 (Distribution Map in Annex 1)
VENTILATION SYSTEM 840 # Technical Name: Ventilator Pressure and Volume # Registration: 101398100...
  • Modelo / Serial
  • Manufacturer
    COVIDIEN LLC.; MALLINCKRODT DO BRASIL LTDA
  • 1 Event
    • Alerta De Seguridad para VENTILATION SYSTEM 840 # Technical Name: Ventilator Pressure and Volume # Registration: 10139810058 # Hazard Class: III - HIGH RISK # Product Code: 4-075907-00 # AFFECTED SERIES: Serial numbers including sequence from 3510012377 to 4200000001 #
Ventilation support system BIPAP, Bipap Auto SV, registration 80102510425, risk class II, all bat...
  • Modelo / Serial
  • Manufacturer
    VR Medical Importadora e Distribuidora de Produtos Médicos; Respironics Inc. (Currently Philips Respironics)
  • 1 Event
    • Alerta De Seguridad para Ventilation support system BIPAP, Bipap Auto SV, registration 80102510425, risk class II, all batches.
Vent Edwards cannula. Models at risk: E060, E061, PE062. Anvisa Registry n ° 80219050029.
  • Modelo / Serial
  • Manufacturer
    Edwards Lifescience Comércio de Produtos Ltda.; Edwards Lifesciences LLC
  • 1 Event
    • Alerta De Seguridad para Vent Edwards cannula. Models at risk: E060, E061, PE062. Anvisa Registry n ° 80219050029.
Ventak Prizm 2 DR, Contak Renewal and Contak Renewal 2 CRT-Ds, Ventak Prizm AVT, Vitality AVT, Re...
  • Modelo / Serial
  • Clasificación del producto
    Cardiovascular Devices
  • Manufacturer
    Guidant Corporation/EUA
  • 1 Event
    • Alerta De Seguridad para Ventak Prizm 2 DR, Contak Renewal and Contak Renewal 2 CRT-Ds, Ventak Prizm AVT, Vitality AVT, Renewal 2 AVT and Renewal 4 AVT.
VENOUS CANAL SARNS / ANVISA Registry n ° 80012280001 ;. ARTERIAL CANAL SARNS / ANVISA Registry n ...
  • Modelo / Serial
  • Manufacturer
    Terumo Cardiovascular System Corporation
  • 1 Event
    • Alerta De Seguridad para VENOUS CANAL SARNS / ANVISA Registry n ° 80012280001 ;. ARTERIAL CANAL SARNS / ANVISA Registry n ° 80012280011.
VENOSA CANAL SARNS. Model: VENOUS CRANE MVD DOUBLE CROSS STAGE 4934; 4935; 4936. Anvisa Registry ...
  • Modelo / Serial
  • Manufacturer
    Terumo Cardiovascular System Corporation; Terumo Medical do Brasil Ltda.
  • 1 Event
    • Alerta De Seguridad para VENOSA CANAL SARNS. Model: VENOUS CRANE MVD DOUBLE CROSS STAGE 4934; 4935; 4936. Anvisa Registry n ° 80012280011.
Vascular Graft Prosthesis: (1) Distaflo Bypass, (2) Flexible with Small Bubble. Catalog No. (1) D...
  • Modelo / Serial
  • Manufacturer
    IMPRA Inc Div C R Bard Inc
  • 1 Event
    • Alerta De Seguridad para Vascular Graft Prosthesis: (1) Distaflo Bypass, (2) Flexible with Small Bubble. Catalog No. (1) DF5006SC, DF5007SC, DF6006SC, DF6007SC, DF7006SC, DF8006SC; (2) F1006TWS, F3006TWSC, F310086TWS, F310086TWSC, F5006S, F5006SC, F5006TWS, F5006TWSC, F5008S, F5008TWS, F5008TWSC, F6006TWS, F6006TWSC, F7004TWS, F7005TWS, F7005TWSC, F7006S, F7006SC, F7006TWS, F7006TWSC, F7007TWS, F7007TWSC, F7008S, F7008SC , F7008TWS, F7008TWS, F7008TWS, F70N75TSC, F70N75TWS, F70T74TSC, F70T74TWS, F70T85TWS, F70T85TWS, F8006S, F8006SC, F8006TWS, F8007TWS, F8007TWS, F8007TWSC, F8008S, F8008SC, F8008TWS, F8008TWSC
VARIOUS PRODUCTS /// 1.Commercial Name: Knee Prosthesis - Registration: 10108770064 - Risk Class:...
  • Modelo / Serial
  • Manufacturer
    IMPOL INSTRUMENTAL E IMPLANTES LTDA
  • 1 Event
    • Alerta De Seguridad para VARIOUS PRODUCTS /// 1.Commercial Name: Knee Prosthesis - Registration: 10108770064 - Risk Class: III - Models and Lots in ANNEX; /// 2.Commercial Name: Spongy Screw - Registration: 10108770074 - Risk Class: III - Models and Lots in ANNEX; /// 3. Trade Name: Shoulder Prosthesis - Registration: 10108770083 - Risk Class: III - Models and Lots in ANNEX; /// 4. Trade Name: NON-CONVENTIONAL ENDOPROTES FOR TIBIA, FEMUR OR UMERO - Registration: 10108770086 - 5. PRODUCT NAME: FEMALE COMPONENT IMPOL - Registration: 10108770089 - Risk Class: III - Models and Lots in ANNEX; /// 6. Trade Name: FEMALE COMPONENT IMPOL - Registration: 10108770089 - Risk Class: III - Models and Lots in ANNEX; /// 7. Trade Name: SLIDING SCREW - Registration: 10108770090 - Risk Class: III - Models and Lots in ANNEX; Name of Product: Tibial Metallic Base - Registration: 10108770091 - Risk Class: III - Models and Lots in ANNEX; /// 9. Trade Name: CORTICAL SCREW - Registration: 10108770092 - Risk Class: III - Models and Lots in ANNEX; /// 10. Trade Name: PLACA TUBO LARGE FRAGMENTS - Registration: 10108770094 - Risk Class: III - Models and Lots in ANNEX; /// 11. Trade Name: RETAIL PLATE - Registration: 10108770095 - Risk Class: III - Models and Lots in ANNEX; /// 12. Trade Name: MODULAR FEMALE HEAD IN STEEL - Registration: 10108770096 - Hazard Class: III - Model and Lots in ANNEX; /// 13. Trade Name: PROTEIN OF ELBOW FOR ARTHROPLASTY UMERO-ULNAR TOTAL CEMENTED - Registration: 10108770097 - Risk Class: III - Models and Lots in ANNEX; /// 14. Trade Name: Intramedine haste BLOCKED - Registration: 10108770099 - Risk Class: III - Models and Lots in ANNEX; /// 15. Trade Name: MODIFIED CEMENT FEMALE STEM - Registration: 10108770106 - Risk Class: III - Models and Lots in ANNEX; // 16. Trade Name: ACETABULAR COMPONENT IN CEMENTED POLYETHYLENE - Registration: 10108770107 - Risk Class: III - Models and Lots in ANNEX; /// 17. Trade Name: System for total knee prosthesis - Registration: 10108770108 - Class of Risk: III - Models and Lots in ANNEX; /// 18. Trade Name: SYSTEM FOR PARTIAL ARTHROPLASTY V GENERATION - Registration: 10108770109 - Hazard Class: III - Models and Lots in ANNEX; /// 19. Trade Name: POLYMERIC ACETABULAR NUCLEUS WITH METALLIC JOINT SURFACE - Registration: 10108770111 - Hazard Class: III - Models and Lots in ANNEX ; /// 20. Trade Name: PINO DE SCHANZ - Registration: 10108770114 - Risk Class: III - Models and Lots in ANNEX; /// 21. Trade Name: Head for Integral Shoulder Arthroplasty - Registration: 10108770115 - Class of /// 22. Trade Name: FIXATION SYSTEM FOR THE LARGE AND SMALL SPACES OF STAINLESS STEEL FRAGMENTS - IMPOL - Registration: 10108770117 - Risk Class: III - Models and Lots in ANNEX ; /// 23. Trade Name: ENDOPROTESES INFERIOR MEMBERS EUROTOP - Registration: 10108770118 - Risk Class: III - Models and Lots in ANNEX; /// 24. Trade Name: Modular System for Shoulder Arthroplasty Eccentra II - Registry: 10108770122 - Risk Class: III - Models and Lots in ANNEX; / 25. Trade Name: INSERTO TIBIAL - IMPOL - Registration: 10108770123 - Class of Risk: III - Models and Lots in ANNEX; /// 26. Trade Name: INSERTO TIBIAL - IMPOL - Models and Lots in ANNEX; /// 27. Trade Name: Large and Small Blocked Regional Special Panels System - Impol - Registration: 10108770125 - Risk Class: III - Models and Lots in ANNEX; ///
VANG VITROS REAGENT KIT Technical Name: VANCOMICINE ANVISA Registration Number: 80145900812 Hazar...
  • Modelo / Serial
  • Manufacturer
    Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda; Ortho-Clinical Diagnostics, Inc.
  • 1 Event
    • Alerta De Seguridad para VANG VITROS REAGENT KIT Technical Name: VANCOMICINE ANVISA Registration Number: 80145900812 Hazard Class: II Affected Model: Box with 6 kits (Reagent 1: 9.7ml / Reagent 2: 4.9ml) Lot / Serial Numbers affected: SKU 6801709, lot 315506
VAMP Jr. Edwards Blood Collection Closed System, model VMP306, Anvisa Registration No. 8021905005...
  • Modelo / Serial
  • Manufacturer
    Edwards Lifesciences Comércio de Produtos Médico-Cirúrgicos Ltda
  • 1 Event
    • Alerta De Seguridad para VAMP Jr. Edwards Blood Collection Closed System, model VMP306, Anvisa Registration No. 80219050051, manufactured until 02/29/2008.
VALP VITROS REAGENT KIT. Anvisa Registry: 80145900779. Affected lots: 149776 and 141094.
  • Modelo / Serial
  • Manufacturer
    Johnson & Johnson Medical Brasil Ltda.; Ortho Clinical Diagnostics.
  • 1 Event
    • Alerta De Seguridad para VALP VITROS REAGENT KIT. Anvisa Registry: 80145900779. Affected lots: 149776 and 141094.
Valleylab Cool-Tip RF electrode and auxiliaries - MS Registry: 10349000258. Affected lots - see a...
  • Modelo / Serial
  • Manufacturer
    AUTO SUTURE DO BRASIL LTDA
  • 1 Event
    • Alerta De Seguridad para Valleylab Cool-Tip RF electrode and auxiliaries - MS Registry: 10349000258. Affected lots - see annex. http://en.wikipedia.org/w/eng/wiki/index.php
VACUTAINER - TUBES FOR COMBUSTIBLE BLOOD COLLECTION - Reg. 10033430136. BD VACUTAINER GLASS TUBE ...
  • Modelo / Serial
  • Manufacturer
    BECTON DICKINSON INDS CIRURGICAS LTDA
  • 1 Event
    • Alerta De Seguridad para VACUTAINER - TUBES FOR COMBUSTIBLE BLOOD COLLECTION - Reg. 10033430136. BD VACUTAINER GLASS TUBE WITH BLOOD PARAGLIDER REAGENT - Reg. 10033430313. BD VACUTAINER PLASTIC TUBE WITH BLOOD PARAGLIDER REAGENT - Reg.10033430261. TUBO VACUTAINER BD - Reg.10033430014
USP 0.25 mg / ml. injection of Digoxin in 1 ml of Tubex cartridges; (2) USP 50 mg / ml. injection...
  • Modelo / Serial
  • Manufacturer
    Wyeth-Ayerst Laboratories
  • 1 Event
    • Alerta De Seguridad para USP 0.25 mg / ml. injection of Digoxin in 1 ml of Tubex cartridges; (2) USP 50 mg / ml. injection of Dimenhydrin in 1 ml. of cartridges Tubex; (3) USP 50 mg / ml. of Difenidramine HCI injection in 1 ml. of Tubex cartridges .. Lots Nos .: (1) 4990194, (2) 49990197, (3) 49990052
USER'S MANUAL FOR ECLIPSE TMR 2000 LASER SYSTEMS. SYSTEM SERIES NUMBERS: 20103, 20106, 20107, 201...
  • Modelo / Serial
  • Manufacturer
    TECNOLOGIAS CIRÚRGICAS ECLIPSE INC.
  • 1 Event
    • Alerta De Seguridad para USER'S MANUAL FOR ECLIPSE TMR 2000 LASER SYSTEMS. SYSTEM SERIES NUMBERS: 20103, 20106, 20107, 20114, 20119 To 20150 , 2014, 20158 to 20160, 20164, 20165, 20202 to 20204, 20209, 20211, 20230, 20231, 20234, 20250 to 20254, 20260, 20264 to 20268, 20270 to 20273, 20278, 20279, 20283, 20286, 20287 to 20290 , 20293 to 20297, 20303 to 20317, 20319, 20321 to 20327, 20333 to 20487, 40103, 40106, 40107, 40110, 40112 to 40114, 40116.
Urological Tables HydraVision System Hydradjust IV (HydraVision System Hydradjust IV Urological T...
  • Modelo / Serial
  • Manufacturer
    Liebel-Flarsheim Business/Mallinckrodt Inc
  • 1 Event
    • Alerta De Seguridad para Urological Tables HydraVision System Hydradjust IV (HydraVision System Hydradjust IV Urological Tables): (1) Reverse, (2) Reverse with color monitor, (3) Reverse for Right Volume, (4) Reverse Volume, 3, (6) Standard Color Monitor, (7) Standard Left, (8) Standard Volume, (9) Standard Color Monitor, (10) Standard W / 4: 3, (11) Reverse Volume; Hydradjust with Urological Tables: (12) Left Fixed Color Monitor, (13) Fixed Right. Parts Nos .: (1) 400001, (2) 400005, (3) 400017, (4) 400011, (5) 400007, (6) 400006, (7) 400002, (8) 4,00012, (9) 10) 400008, (11) 400015, (12) 400026, (13) 400025; Series No.s .: (1 to 11) all serial numbers; (12) 0297-0520, 0397-0521, 0397-0523, 0797-0501, 1196-0502, 3496-0505, 3596-0508, 3996-0511, 4796-0515; (13) 0397-0522, 0397-0524, 3496-0503, 3496-0504, 3596-0506, 3596-0507, 3896-0510, 4596-0512, 4796-0513, 4796-0514, 5196-0516 to 5196-0518 , 5296-0519
UROLOGICAL TABLES
  • Modelo / Serial
  • Manufacturer
    N/A
  • 1 Event
    • Alerta De Seguridad para UROLOGICAL TABLES
URINE TEST TAPES CHEMSTRIP9
  • Modelo / Serial
  • Manufacturer
    ROCHE DIAGNÓSTICOS CORP. SUB F HOFFMANN-LA ROCHE LTDA
  • 1 Event
    • Alerta De Seguridad para URINE TEST TAPES CHEMSTRIP9
URINE SOLIDOR COLLECTOR - Record 10237580033 - Lots Affected 1203B and 1235A.
  • Modelo / Serial
  • Manufacturer
    LAMEDID COMERCIAL E SERVICOS LTDA
  • 1 Event
    • Alerta De Seguridad para URINE SOLIDOR COLLECTOR - Record 10237580033 - Lots Affected 1203B and 1235A.
URINE DRAIN BAG CLOSED SYSTEM, REGISTRATION 10342310043, RISK CLASS I, CLT-33 MODEL, FLEXOR MARK,...
  • Modelo / Serial
  • Manufacturer
    Flexor Industrial e Comercial Eireli
  • 1 Event
    • Alerta De Seguridad para URINE DRAIN BAG CLOSED SYSTEM, REGISTRATION 10342310043, RISK CLASS I, CLT-33 MODEL, FLEXOR MARK, COLEFLEX STANDARD; COLEFLEX CLASSIC; COLEFLEX FOR PERNAS.Lote 151017.
Urine drainage bag Closed system, model CLT-47, registration number 10342310043, hazard class I. ...
  • Modelo / Serial
  • Manufacturer
    Flexor Industrial e Comercial Eireli
  • 1 Event
    • Alerta De Seguridad para Urine drainage bag Closed system, model CLT-47, registration number 10342310043, hazard class I. Lot: 151208.
Urine collector for male urinary incontinence; Brand EMBRAMED; Model no. 06, Record: 10252420035....
  • Modelo / Serial
  • Manufacturer
    Embramed Ltda.; Embramed Indústri e Comércio de Produtos Hospitalares Ltda.
  • 1 Event
    • Alerta De Seguridad para Urine collector for male urinary incontinence; Brand EMBRAMED; Model no. 06, Record: 10252420035. Batch numbers affected: attached.
URIC ACID / UIC ACID, List No. 7D76, Lot Number 95015HWOO. Registration number: 10055310819
  • Modelo / Serial
  • Manufacturer
    Abbott-Divisão Diagnósticos
  • 1 Event
    • Alerta De Seguridad para URIC ACID / UIC ACID, List No. 7D76, Lot Number 95015HWOO. Registration number: 10055310819
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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.

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