International safety notice
Alert 2550 (Technosurveillance) Diamed - Diaclon ID-Card Abo/D + Reverse Test Possibility of occurrence of a weak non-specific reaction of the product.
Brazil / Anvisa · BRA · Apr 19, 2018
Key facts
| Title | Alert 2550 (Technosurveillance) Diamed - Diaclon ID-Card Abo/D + Reverse Test Possibility of occurrence of a weak non-specific reaction of the product. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: ID-Card Diaclon Abo/D + Reverse Proof Technical name: Immunohematology - ABO - Monoclonal Origin ANVISA registration number: 80004040061 Risk class: IV Affected model: 00 000 000 0012 35 Affected Lot/Series Numbers: Lot: 50092.95.19 - ID-Card numbering sequence from 23,000 to 31,000 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO DIAMED LATINO AMÉRICA SA CNPJ 71015853000145 RUA ALFREDO ALBANO DA COSTA 100 DISTRITO INDUSTRIAL LAGOA SANTA MG TEL 31 36896637 EMAIL BRZRABIORADCOM FABRICANTE DIAMED LATINO AMÉRICA SA CNPJ 71015853000145 RUA ALFREDO ALBANO DA COSTA 100 DISTRITO INDUSTRIAL LAGOA SANTA MG TEL 31 36896637 EMAIL BRZRABIORADCOM |
| Models | 80004040061, 31.000, 50092.95.19, 23.000 |
| Date | Apr 19, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1