International safety notice
Matriz de regeneración dérmica de capa única Integra y Matriz de regeneración dérmica de capa única (delgada) Integra
Spain / AEMPS · ESP · Sep 26, 2019
Key facts
| Title | Matriz de regeneración dérmica de capa única Integra y Matriz de regeneración dérmica de capa única (delgada) Integra |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Matriz de regeneración dérmica de capa única Integra y Matriz de regeneración dérmica de capa única (delgada) Integra |
| Manufacturer | Integra LifeSciences, EEUU. |
| Models | 28022, 14971, 6200020050, NEPMANBH0I, RLÀAI010, 609-936-5499, 444-1122, 64101T, 91.822.52.89, 28938, C2017, 62021 and 17 more |
| Event type | Safety Notice |
| Date | Sep 26, 2019 |
At a glance
- No Recall
- Yes 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