12 results
·
26ms
·
Sources: EU EUDAMED, US FDA
BEAVER R-K KNIFE
FDA 510(k)
FDA Class 1
·Ophthalmic
Vyaire
FDA UDI
Jaeger Medical GmbH·34250892903461·Rebreathing bag 20l
Vyntus
FDA UDI
Jaeger Medical GmbH·34250892901276·Rebreathing bag 20 L
Jaeger
FDA UDI
Jaeger Medical GmbH·34250892907070·Rebreathing bag 20l
Eaglewear
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746008078·HIGH PULL RELEASE MODULE - EAGLEWEAR CLEAR 10/PKG
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209111848·KIT, M-FAK, CUSTOM
Manual Wheelchair (W47)
FDA 510(k)
FDA Class 1
·Physical Medicine
DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT)
FDA 510(k)
FDA Class 2
·Cardiovascular
UNSPECIFIED SAFESET TRANSPAC SETS
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025
OT PING ENHANCED METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014
PCA EMPTY STERILE
FDA Adverse Event
Malfunction
·HOSPIRA INC.·Product code MEA·November 27, 2012
LIGACLIP CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 18, 2015