International safety notice
Alteration of the Instructions For Use for EndoFit Pre-loaded Thoracic Stent Graft from LeMaitre
Germany / BfArM · DEU · May 2, 2005
Key facts
| Title | Alteration of the Instructions For Use for EndoFit Pre-loaded Thoracic Stent Graft from LeMaitre |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | EndoFit Pre-loaded Thoracic Stent Graft from LeMaitre |
| Manufacturer | Alteration of the Instructions For Use for EndoFit Pre-loaded Thoracic Stent Graft from LeMaitre |
| Models | 49-1016196-527072, 221-2223, 2-9-4, 102-0074, 659230, 03-5216-5631, 65812, 22B2266, 01803, 03-5215-5632 |
| Date | May 2, 2005 |
| Regulator page | bfarm.de |
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