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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Accu-Chek Connect Application (iOS) Technical Name: Accu-Chek Connect Application (iOS) Registration Number ANVISA: 10287411061 Hazard Class: Model Affected: Version 1.2.0 for iOS Roche Diagnóstica Brasil Ltda; Roche Diagnostics GmBH Brazil ANVISA
Accu-Chek Connect Application Technical Name: Accu-Chek Connect Application Registration Number ANVISA: 10287411061 Affected Model: Versions 2.0.0, 2.0.1, 2.1.0 (iOS & Android) Roche Diagnóstica Brasil Ltda.; Roche Diabetes Care GMBH Brazil ANVISA
Accu-Chek Connect Application Technical Name: Accu-Chek Connect Application Registration Number ANVISA: Risk Class: Affected Model: Version 1.2.0, 1.2.2 and 2.0.0 (iOS and Android) Serial Numbers Affected: Required update of Accu-Chek Connect Application 1.2.0, 1.2.2, 2.0.0 (iOS and Android) to ensure correct Correction Bolus suggestion. Roche Diagnóstica Brasil Ltda; Roche Diagnostics GmBH Brazil ANVISA
ACCU-CHEK® Hair Glucose Monitor Roche Diagnóstica Brasil Ltda Brazil ANVISA
Accu-Chek Inform II Base Unit and Handheld Base Unit, registry 10287410863, hazard class II, batches affected: 05802151 to 05205301 and 05809021 to 05205311. Roche Diagnóstica Brasil Ltda.; Roche Diagnostics GmBH Brazil ANVISA
Accu-Chek Infusion System, Model: TenderLink, Brand: Roche, Record: 10287411002. Serial / Lot Numbers: 5032438/5033658/5051303/5053292/5065540/5065550. Roche Diagnostica Brasil Ltda; Roche Brazil ANVISA
ACCU CHEK PERFORMA - Registration with Anvisa nº 10287410617 Roche Diagnóstica Brasil Ltda. Brazil ANVISA
Accu-Chek® Spirit and Accu-Chek® Spirit Combo, Registration: 10287410883, Hazard Class III, Serial Numbers: SEE ANNEX. Roche Diagnóstica Brasil Ltda.; Roche Diagnostics GmBH Brazil ANVISA
AccuTrak Intravascular Catheter System DCS (CoreValve System accessory). Anvisa Registry n ° 10339190448. MEDTRONIC COREVALVE LLC; Medtronic Comercial Ltda. Brazil ANVISA
ACETABULAR COMPONENT OF POLYETHYLENE META BIO (registration no. 80034760015), PRÓTESE FOR ARTHROPLASTY OF META BIO HIP - Co-Cr-Mo (registration nº 80034760016) and PRÓTESE FOR ARTHROPLASTY OF META BIO TITÂNIO HIP (registry nº 80034760017). Meta Bio Industrial Ltda. Brazil ANVISA
ACETÁBULO DE MULLER INCOMEPE (Registro Anvisa 10395270012) - LOTE: 018089 INCOMEPE INDÚSTRIA DE MATERIAIS CIRÚRGICOS LTDA - CNPJ: 57.212.870/0001-41. Brazil ANVISA
ACID LACTIC Technical Name: Lactic Acid ANVISA Registration Number: 80146501641 Hazard Class: II Affected Model: Not applicable Serial Numbers Affected: 31497UN14; 09353UN15; 45216UN15; 14596UN15; 37055UN15 and 14782UN16 Abbott Laboratórios do Brasil; Abbott Laboratories Diagnostics Division. Brazil ANVISA
A: CLINICAL CHEMISTRY SYSTEMS WITH SOFTWARE VERSIONS LESS THAN 7.0: (1) MODEL 3332 VITROS 250, (2) MODEL 3391 VITROS 250 AT; B: CLINICAL CHEMISTRY SYSTEMS WITH SOFTWARE VERSIONS LESS THAN 3.07: (3) MODEL 3360 VITROS 950, (4) MODEL 3361 VITROS 950 AT ORTHO-CLINICAL DIAGNOSTICS INC A JOHNSON & JOHNSON CO. Brazil ANVISA
ACRYLIC LENS TECNIS 1 PART MODEL ZCB00. Registro Anvisa 80147060093. Products affected: products with the following expiration dates 05/2011, 06/2011, 07/2011, 08/2011, 09/2011 and 10/2011. Vistatek Produtos Óticos S/A.; Abbott Medical Optics Inc. Brazil ANVISA
Acrysof Cachet Phakic (Intraocular Lens). Anvisa Registry n ° 80147540167. Models at risk: L12500, L13000, L13500 and L14000. Novartis Biociências; Alcon Laboratories, Inc. Brazil ANVISA
ACRYSOF CACHÉT PHAKIC - Models: L12500, L13000, L13500 and L14000. ANVISA registration nº 80147540167 ALCON LABORATORIES, INC Brazil ANVISA
Actifuse ABX 1-2mm, manufacturer Apatech, models 506005078047 (2,5mm); 506005078048 (5.0mm) and 506005078049 (10.0mm). Record 80253610018. Series Affected: See Annex. Osteocamp Implantes e Materiais Cirúrgicos Ltda.; Apatech Limited. Brazil ANVISA
Actin® Activated Cephaloplastin Reagent, 2 x 10 ml Carton - Registration 10345161140 - lots 557128; 5,573,821; 557135 Siemens Healthcare Diagnósticos Ltda. Brazil ANVISA
Actin® Activated Cephaloplastin Reagent, 2 x 10 ml Pack - Registration 10345161140 - lot 557116 Siemens Healthcare Diagnósticos Ltda.; Siemens Healthcare Diagnostics Products GmbH Brazil ANVISA
Acuity Central Physiological Monitoring Station with the following software versions: (1) 4.03.00, (2) 4.03.01, (3) 4.03.02, (4) 4.03.03, (5) 4.03.04, (6) ) 4.03.05; (7) VHF / UHF protocol, wireless, telemetry units. Welch Ally Protocol Inc Div Welch Allyn Inc Brazil ANVISA
ACUSON diagnostic ultrasound system, ACUSON S1000 models; ACUSON S2000, registration 10234230192, hazard class II, with software version VC30A, VC30B, VC30C or VC31A, batches / series: 202134; 210786; 211085; 211397; 211080. Siemens Ltda.,; SIEMENS Medical Solutions USA, Inc.; Siemens Ltda. Brazil ANVISA
ACUSON Diagnostic Ultrasound System. Model: ACUSON S2000. Anvisa Registry n ° 10234230192. Siemens Ltda.; Siemens Medical Solutions USA, Inc. Brazil ANVISA
Acuson Sequoia C512 / C256 / 512 # Series Affected Series Acuson Sequoia C512 / C256 / 512 # Product Name: Acuson Sequoia C512 / C256 / 512 # Product Name: ACUSON SEQUOIA ULTRASONIC SYSTEM # : 40507963, 41008034, 41008038, 41608093 Siemens Ltda.; Siemens Medical Solutions USA, Inc. Brazil ANVISA
ACUSON Ultrasound Diagnostic System Technical Name: Ultrasound Apparatus ANVISA Registration Number: 10345162017 Hazard Class: II Affected Model: ACUSON S1000, ACUSON S2000, ACUSON S3000 Series Affected Numbers: 201092, 201936, 202290, 202295 , 202352, 202637, 203198, 203217, 203217, 203217, 203217, 203282, 203531, 203535, 203549, 203559, 205259, 205260, 205262, 205282, 205344, 205494, 205521, 205572, 205651, 205701, 205750, 205876, 206270 , 206756, 206984. Siemens Healthcare Diagnósticos S.A; Siemens Healthcare Diagnostics Inc. Brazil ANVISA
Acuvue Advance. Technical Name: Contact Lenses. ANVISA registration number: 80148620026. Class of risk: II. Model Affected: N / A. Serial numbers affected: B00DHLP Johnson & Johnson Industrial Ltda; Johnson & Johnson Vision Care, Inc Brazil ANVISA