International safety notice
Disposable Syringe
Brazil / Anvisa · BRA · May 18, 2015
Key facts
| Title | Disposable Syringe |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | MEDRAD syringe for contrast injection Registration: 80172890031, batches 172003; |
| Manufacturer | DETENTOR DO REGISTRO MEDRAD DO BRASIL CNPJ 00506570000158 ENDEREÇO RUA DOMINGOS JORGE 1100 P9604 1 ANDAR SÃO PAULO FABRICANTE MEDRAD INC ESTADOS NIDOS ONE MEDRAR DRIVE INDIANOLA PENSILVANIA 15051 |
| Models | 172005, 172003, 80172890031 |
| Date | May 18, 2015 |
| 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