International safety notice
Technical name: Angled tubular non-absorbable plate for osteosynthesis
Brazil / Anvisa · BRA · Apr 19, 2017
Key facts
| Title | Technical name: Angled tubular non-absorbable plate for osteosynthesis |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: TUBE PLATE SYSTEM FOR BONE SYNTHESIS - MB Technical name: Non-absorbable tubular angled plate for osteosynthesis ANVISA registration number: 80034760050 Risk class: III Affected model: 2266-318-095 Affected serial numbers: 00107967/ 006939 - 08 units - Manufacturing Date: 01/14/2016 00109330/006939 - 08 units - Manufacturing Date: 01/14/2016 00107963/006939 - 11 units - Manufacturing Date: 01/14/2016 00110188/006939 - 11 units - Manufacture date: 01/14/2016 00107966/006939 - 04 units - Manufacture date: 01/14/2016 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO META BIO INDUSTRIAL LTDA AVENIDA 37 1907 BAIRRO ESTÁDIO RIO CLARO SP CNPJ 02513989000162 FABRICANTE META BIO INDUSTRIAL LTDA AVENIDA 37 1907 BAIRRO ESTÁDIO RIO CLARO SP CNPJ 02513989000162 |
| Models | 006939, 00107963, 2266-318-095, 00110188, 00107966, 80034760050, 00107967, 00109330 |
| Date | Apr 19, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 10–99 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