9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NailLift
FDA 510(k)
FDA Unclassified
·Unknown
Ophthalmic Hooks
FDA UDI
KATENA PRODUCTS, INC.·00841668114315·PUSH-PULL HOOK ANGLED (BX/3)
SHOFU BLOCK HC
FDA 510(k)
FDA Class 2
·Dental
COOK GASTRIC SIZING BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CERTAIN TITANIUM HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·December 29, 2020
LONG NAIL KIT R1.5, LEFT 10X260MM X 125
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 16, 2010
NEOPUFF INFANT RESUSCITATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTL·October 28, 2008
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 1, 2011
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013