International safety notice
Alert 2622 (Technosurveillance) - Biomet 3I do Brasil Comércio de Aparelhos Médicos Ltda.
Brazil / Anvisa · BRA · Jul 20, 2018
Key facts
| Title | Alert 2622 (Technosurveillance) - Biomet 3I do Brasil Comércio de Aparelhos Médicos Ltda. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Non-Sterile Non-Sharp Non-Hingulated Instruments with Biomet Orthopedics Trauma Connection Technical Name: Instrumental for Orthopedic Implant ANVISA registration number: 80044680179 Risk Class: I Affected model: 14-442093 Affected serial numbers: 740620 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BIOMET 3I DO BRASIL COMÉRCIO DE APARELHOS MÉDICOS LTDA RUA MACHADO BITTENCOURT Nº 361 12º ANDAR SÃO PAULO SP TEL 11 35681339 EMAIL ANAHAASZIMMERBIOMETCOM FABRICANTE DO PRODUTO BIOMET TRAUMA 56 EAST BELL DRIVE WARSAW IN ESTADOS UNIDOS DA AMÉRICA |
| Models | 80044680179, 14-442093, 740620 |
| Date | Jul 20, 2018 |
| 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