International safety notice
IMPLANT
Brazil / Anvisa · BRA · Feb 1, 2016
Key facts
| Title | IMPLANT |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Knee Arthroplasty/Knee Prosthesis System; |
| Manufacturer | DETENTOR DO REGISTRO MEDSINTESE IMPORTAÇÃO EXPORTAÇÃO E COMÉRCIO EIRELI ENDEREÇO RUA BATATA RIBEIRO 190 CJS 414546 71 AO 76 E 8184 SÃO PAULOSP FABRICANTE ZIMMER INC 1800 WEST CENTER STREET WARSAW INDIANA 465821 EUA |
| Models | 62041152, 61988031, 62005748, 61850057, 61801529, 61831823, 61822616, 62128274, 61824682, 62054626, 6307-00-008, 61831831 and 9 more |
| Date | Feb 1, 2016 |
| 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