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  • Dispositivo 960
  • Fabricante 297
  • Evento 124969
  • Implante 79
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Hemodialysis Machine, Dialog + and Dialog + HDF models online (7102005, 7102072, 710200C and 710207E), registration 80136990498, risk class III, various series (SEE ANNEX). Laboratórios B. Braun S.A. Endereço; B. Braun Avitum AG Brazil ANVISA
Trade Name: Closed System Urine Collection Fellowships Technical Name: Collectors ANVISA Registration Number: 80136990508 Hazard Class: I Model Affected: UREOFIX 500 CLASSIC, EB. 2.0L, TUBE 120CM (4417930) Serial numbers affected: Item 4417930 / lot: 16F01E8SUA. Laboratórios B. Braun S.A.; B. Braun Melsungen AG Brazil ANVISA
Spinocath - Spinal Anesthesia Kit Technical Name: Anesthesia Kit ANVISA Registration Number: 10008530204 Hazard Class: II Affected Model: 4517725 Serial numbers Affected: lot: 2I20018501 Laboratórios B. Braun S.A.; B. Braun Melsungen AG Brazil ANVISA
Name of the manufacturer: Generators Technical name: LEKTRAFUSE HF GENERATOR BIPOLAR Registration number ANVISA: 80136990815 Hazard class: III Affected model: GN200 Affected serial numbers: 2028, 2054, 2060, 2065, 2066, 2071, 2070, 2072, 2074, 2075 , 2077, 2079, 2081, 2083, 2089, 2094, 2149, 2151, 2152, 2153, 2155, 2156, 2172. Laboratórios B. Braun S.A.; Aesculap AG Tuttlingen (AAG) Brazil ANVISA
Hemodialysis Machine Technical Name: ANVISA Registration Number: 80136990498 Hazard Class: III Affected Model: Dialog + and Dialog + HDF online (710200C, 7102072, 7105005 and 710500C) Laboratórios B. Braun S.A.; B. Braun Avitum AG Brazil ANVISA
Infusomat Compact - Infusomat Compact Infusion Pump / Infusion Pump Technical Name: Infusion Pump ANVISA Registration Number: 10008530367 Hazard Class: III Model Affected: Infusomat compact Laboratórios B. Braun S.A.; Laboratórios B. Braun S.A. Brazil ANVISA
CERTOFIX DUO V 720 JUG 7F and CERTOFIX DUO V 730 SUB 7F Technical name: FAMILY OF CENTRAL VENOUS CATHETERS ANVISA Registration Number: 80136990671 Hazard Class: IV Affected Model: 4161211 and 4161319 Serial Numbers Affected: 16M15A8551 and 16M21A8551 Laboratórios B. Braun S.A.; B. Braun Melsungen AG Brazil ANVISA
Trade name: Broca Esf. Diam. Hi-Line Great. Thick IT / Drill Esf. Diam. Hi-Line Great. Thick Tip Technical Name: Broca Esf. Diam. Hi-Line Great. Thick IT / Drill Esf. Diam. Hi-Line Great. Affected serial numbers: 51745118, 51649830, 51708484, 51838047, 51634741 and 51293170. Note: The unit of lot 51293170 was used during the disclosure project. of the product in 2005, and is not distributed to the customer. Laboratórios B. Braun S.A.; Aesculap AG Brazil ANVISA
Name of INTRAFIX PRIMELINE AIR IL Technical Name: Family of Gravitational Infusion Equipment for Parental Solutions and Medications ANVISA Registration Number: 80136990540 Hazard Class: II Model Affected: 401450P Serial Numbers Affected: 17A20LB026 Laboratórios B. Braun S.A. Brazil ANVISA
Commercial Name: Atlas Gold Dilatation Catheter. Technical name: Columbus rev. Spacer Fémoral post.f6 15mm / Columbus rev. Spacer Fémoral post. f7 15mm. ANVISA registration number: 80136990668. Risk class: III. Model Affected: NR586K / NR587K. Serial numbers affected: Code NR586K: 51586634 and 51447596; Code NR587K: 51585136 and 51447597 Laboratórios B. Braun S.A.; Aesculap AG Brazil ANVISA
Trade name: DS Aesculap Titanium Clips and DS Clip Clips. Technical name: DS Aesculap Titanium Clips and DS Clip Clips. ANVISA registration number: 80136990853. Class of risk: III. Affected Model: FC230R, PL462SU, PL465SU, PL468SU, PL471SU, PL475SU, PL807R, PL808R, PL809R, PL817R, PL818R. Affected serial numbers: The field action involves all batches of product, since it is a change in the "Contraindications" field of the Instructions for Use. Laboratórios B. Braun S.A.; Aesculap AG Brazil ANVISA
Trade name: Askina Calgitrol Paste 15 gr and Askina Gel 15 gr. Technical name: Askina Calgitrol Paste 15 gr and Askina Gel 15 gr. ANVISA registration number: 80136990789. Risk class: III. Affected template: 6241505, 001419SBR and 001419S. Affected serial numbers: Code 001419S: 514031, 514033 and 518472 ;. Code 001419SBR: 485431, 504281, 485431 and 504281 ;. Code 6241505: P2408, P2460, P2469, P2481, P2524, P2528, P2549, P2552, P2556 and P2577. " Laboratórios B. Braun S.A.; B.Braun Melsungen AG Brazil ANVISA
Trade name: Aesculap single use bipolar instrument. Technical name: Aesculap single use bipolar instrument. ANVISA registration number: 80136990832. Risk class: III. Model affected: Caiman 5 mm. Affected Batches / Series Numbers: See Attachment "List of Batches Under Risk" Laboratórios B. Braun S.A.; Aesculap AG Brazil ANVISA
APPLYING FORCEPS FOR YASARGIL ANEURYSM CLIPS Neurological Devices AESCULAP AG Canada HC
PRIMARY ADDITIV ADMINISTRATION SETS WITH CHECK VALVE B. BRAUN MEDICAL INC. Canada HC
S4 OCCIPITAL CERVICAL SPINAL SYSTEM - OCCIPITAL PLATE AESCULAP IMPLANT SYSTEMS LLC Canada HC
VISTA PUMP METRISET BURETTE SETS B. BRAUN MEDICAL INC. Canada HC
NEEDLE FREE DISPENSING PINS B. BRAUN MEDICAL INC. Canada HC
CURLIN 4000 PUMP KIT B. BRAUN MEDICAL INC. Canada HC
OUTLOOK SAFETY INFUSION SYSTEM B. BRAUN MEDICAL INC. Canada HC
ZIRCONIUM ALLOY FEMORAL HEAD AESCULAP IMPLANT SYSTEMS LLC Canada HC
DIALOG+ ONLINE DIALYSIS MACHINES B. BRAUN AVITUM AG Canada HC
DIACAN FISTULA NEEDLE B. BRAUN AVITUM AG Canada HC
DS CLIP APPLIERS AESCULAP AG Canada HC
MINOP INVENT TROCAR 30 AESCULAP AG Canada HC
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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.