International safety notice
TM Ardis Interbody System Inserter
Swiss / SwissMedic · CHE · Apr 22, 2013
Key facts
| Title | TM Ardis Interbody System Inserter |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | TM Ardis Interbody System Inserter |
| Manufacturer | Zimmer, Inc. |
| Models | 06.02338.011, 96-701-10001, 05.Octobre.2012, 512-918-2700, L1607, 09.04.2013, 78727, 55439, 2.12-1, 97-701-10001, 952-832-5600 |
| Event type | Safety Notice |
| Date | Apr 22, 2013 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes 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