FORCEPS, ENT
FDA product code KAE · Class 1 · 10 devices · 5 reports · 7 devices named in recalls
- AESCULAP BH951RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH957RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH959RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH961RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH963RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH965RAesculap AG · FORCEPS, ENT1 recall0 reports
- AESCULAP BH952RAesculap AG · FORCEPS, ENT1 recall0 reports
- Integra® 3711063Integra Lifesciences Production Corporation · FORCEPS, ENT2 reports
- V. Mueller RH551-111Steris Corporation · FORCEPS, ENT2 reports
- Integra® 3711062Integra Lifesciences Production Corporation · FORCEPS, ENT1 report