International safety notice
Technical name: Dehydroepiandrosterone Sulfate (DHEA-S)
Brazil / Anvisa · BRA · Jan 11, 2017
Key facts
| Title | Technical name: Dehydroepiandrosterone Sulfate (DHEA-S) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Nome comercial: Architect Dhea-S Reagent Kit / Architect Dhea-S Kit Reagente Technical name: Dehydroepiandrosterone Sulfate (DHEA-S) ANVISA registration number: 80146501346 Risk class: II Affected model: Not applicable. Affected serial numbers: 01316K000; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ABBOTT LABORATÓRIOS DO BRASIL LTDA CNPJ 56998701000116 RUA MICHIGAN 735 CIDADE MONÇÕES SÃO PAULO SP FABRICANTE ABBOTT GMBH CO KG MAXPLANCKRING 2 65205 WIESBADEN ALEMANHA TELEFONE 224 6681923 FAX 224 6681924 EMAIL ALBERT CHIANELLO |
| Models | 02217C000, 00517F000, 02317D000, 01117A000, 02417D000, 01316K000, 02217D000, 04117H000, 80146501346, 01217A000, 01216K000 |
| Date | Jan 11, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
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