International safety notice
Technical name: System for total multicompartmental femoro-tibio-patellar arthroplasty
Brazil / Anvisa · BRA · Mar 6, 2017
Key facts
| Title | Technical name: System for total multicompartmental femoro-tibio-patellar arthroplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: PROFEMUR RENAISSANCE/LINEAGE TOTAL HIP SYSTEM Technical name: Femoro-tibio-patellar multicompartmental total arthroplasty system ANVISA registration number: 80102511373 Risk class: III Affected model: 36 mm alumina ceramic heads Affected serial numbers: 0211313520; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA ENDEREÇO RUA BATATAES 391 CONJUNTOS 11 13 R 8ºANDAR TELEFONE 11 38857633 FABRICANTE MICROPORT ORTHOPEDICS INC ENDEREÇO 5677 AIRLINE ROAD ALINGTON TN 38002 TELEFONE 55 1126900336 |
| Models | 0657633801, 0211313520, 065ª05810312, 1655972, 1633530, 0557332101, 15541511687588, 1656049, 0311327277, 1655960, 14519031660611, 1555038 and 17 more |
| Date | Mar 6, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 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