22 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Chartis Precision Catheter
FDA 510(k)
FDA Class 2
·Anesthesiology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517569875·CoRoent Ant TLIF Ti, 12x12x34mm 0°
HEALIX TRANSTEND ORTHOCORD PERCANNULA
FDA UDI
Medos International Sàrl·10886705023882·HEALIX TRANSTEND(PEEK/2) Implant System (2) PEE...
Green Sprouts
FDA UDI
O2cool, LLC·00715418095172·Cooling Teether-Purple Grape-3mo+
Pinnacle
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730010070·Pinnacle .022 MC(0T) UL3 0T 8A 0O (10PK)
Green Sprouts
FDA UDI
O2cool, LLC·00715418020341·Cool Fruit Teether-Assorted-3mo+
Green Sprouts
FDA UDI
O2cool, LLC·00715418028606·Cool Fruit Teether-Green Apple-3mo+
Marquis
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730012500·Marquis MBT 022 UL3 Rx 0 Tor. +8 Ang (10PK)
Votion
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730008244·Votion .022 MC(0T) UL3 0T 8A 0O (10PK)
Pinnacle®
FDA UDI
Ortho Organizers, Inc.·00190707112028·Pinnacle .022 MC(0T) UL3 0T 8A 0O (10PK) PINNACLE
Votion®
FDA UDI
Ortho Organizers, Inc.·00190707113933·Votion .022 MC(0T) UL3 0T 8A 0O (10PK) VOTION
Green Sprouts
FDA UDI
O2cool, LLC·00715418028590·
TRAVELAIR PORTABLE COMPRESSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
PRODIGY CHOICE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
FLEXTEND IS-1 BI POSITIVE FIX
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code DTB·August 9, 2006
OT VERIO FLEX METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 19, 2017
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 4, 2014
CONTOUR TEST STRIPS
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·July 15, 2011
PINN MULTIHOLE W/GRIPTION 58MM
FDA Adverse Event
Injury
·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code LPH·July 12, 2013
VANGUARD FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 27, 2017