International safety notice
GDC DETACHABLE SPIRAL MICROMOPLE
Brazil / Anvisa · BRA · Apr 11, 2016
Key facts
| Title | GDC DETACHABLE SPIRAL MICROMOPLE |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: GDC 360° ANVISA registration number: 80005430270 Risk class: IV Maximum Risk Affected models/batches: - Model: M0033471020SR0, lots: 17328407, 17581672, 18617200; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO STRYKER DO BRASIL LTDA CNPJ 02966317000102 RUA URUSSUÍ 300 7º ANDAR SÃO PAULOSP TELEFONE 11 51892503 EMAIL QUALIDADESTRYKERCOM FABRICANTE STRYKER NEUROVASCULAR BUSINESS AND TECHNOLOGY PARK MODEL FARM ROAD CORK IRLANDA TELEFONE 5104132670 EMAIL TARALOPEZSTRYKERCOM |
| Models | 17328407, 80005430270, 17581672, 18617200, M0033471020SR0, 17735100, M00334811300, 17818842 |
| Date | Apr 11, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 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