International safety notice
Technical name: E-test Ertapenem
Brazil / Anvisa · BRA · Apr 25, 2017
Key facts
| Title | Technical name: E-test Ertapenem |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: E-test Ertapenem Technical name: E-test Ertapenem ANVISA registration number: 10158120623 Risk class: II Affected model: Not applicable Affected serial numbers: 1003523980 / 1003528910 / 1004390590 / 1004577410 / 1004624930 / 10048 72750 / 1004886970 / 1005177360 / 1005208910 / 1005183510 and 1005353450 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BIOMÉRIEUX BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS LABORATORIAS LTDA CNPJ 33040635000171 ESTRADA DO MAPUA 491 LOTE 1 TAQUARA JACAREPAGUÁ RIO DE JANEIRO RJ TEL 21 24441415 EMAIL SUELENSILVABIOMERIEUXCOM FABRICANTE BIOMÉRIEUX SA FRANÇA 3 CHEMIN DU PORT MICHAUD 38390 LA BALME LES GROTTES TEL 33478877422 33489430005 EMAIL SOPHIEDUCONGEREXTBIOMERIEUXCOM |
| Models | 1005208910, 1004624930, 1005183510, 1004872750, 1003528910, 1005353450, 1003523980, 1004390590, 1005177360, 10158120623, 1004577410, 1004886970 |
| Date | Apr 25, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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