International safety notice
Matriz de colágeno para la reconstrucción de partes blandas: SurgiMend PRS, SurgiMend PRS Meshed, SurgiMend, SurgiMend MP. Soporte de reparación dérmica: PriMatrix, PriMatrix Ag Antimicrobial. Ver referencias en tabla 1 de la nota de aviso de la empresa
Spain / AEMPS · ESP · Jun 8, 2023
Key facts
| Title | Matriz de colágeno para la reconstrucción de partes blandas: SurgiMend PRS, SurgiMend PRS Meshed, SurgiMend, SurgiMend MP. Soporte de reparación dérmica: PriMatrix, PriMatrix Ag Antimicrobial. Ver referencias en tabla 1 de la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Matriz de colágeno para la reconstrucción de partes blandas: SurgiMend PRS, SurgiMend PRS Meshed, SurgiMend, SurgiMend MP. Soporte de reparación dérmica: PriMatrix, PriMatrix Ag Antimicrobial. Ver referencias en tabla 1 de la nota de aviso de la empresa |
| Manufacturer | TEI Biosciences Inc; EE UU |
| Models | 606-206-003, 606-001-015, 606-400-009, 606-004-107, 10381780113539, 606-400-004, 607-101-225, 607-001-125, 10381780112631, 606-206-006, 606-300-002, 10381780113119 and 256 more |
| Event type | Safety Notice |
| Date | Jun 8, 2023 |
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