109 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Bio2 Technologies
FDA UDI
BIO2 TECHNOLOGIES, INC.·B01010000391·VITRIUM E
18 x 9
CoRoent
FDA UDI
Nuvasive, Inc.·00887517406194·CoRoent LI Inserter, Short
Tempo
FDA UDI
i-SENS, Inc.·00810011730069·Tempo lancet (50T/pack)
AeroPace Handheld Controller
FDA UDI
Lungpacer Medical USA Inc.·00810073210042·
QB1 NMES System
FDA UDI
Motive Health, Inc.·00854816006141·QB1 NMES System; SMALL, SHORT, LEFT
Panama™
FDA UDI
FLOSPINE LLC·B1830830000390·3-Level, 39mm Cervical Plate
Canaveral®
FDA UDI
FLOSPINE LLC·B183170000390·Screw Tap, 9.5mm
SINGLE SIZE TENDON SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
SPIRAL RADIUS RODDING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
6000039-2001-00055
FDA Adverse Event
Injury
·Product code LIT·December 13, 2001
NAVIGUIDE GUIDE WIRE
FDA Adverse Event
Injury
·MEDI-TECH·Product code DQX·July 23, 1998
NAVIGUIDE GUIDE WIRE
FDA Adverse Event
Injury
·MEDI-TECH·Product code DQX·July 23, 1998
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·THE AMPLATZER(R) SEPTAL OCCLUDER (ASO) AND THE AMPLATZER EXCHANGE SYSTEM
OCCLUSION BALLOON CATHETER
FDA Adverse Event
Injury
·MEDI-TECH·Product code LIT·July 20, 2000
OCCLUSION BALLOON CATHETER
FDA Adverse Event
Malfunction
·MEDI-TECH·Product code LIT·July 20, 2000
ARCHITECT IPTH
FDA Adverse Event
Malfunction
·ABBOTT GERMANY·Product code CEW·March 12, 2013
SOFT-VU ANGIOGRAPHIC CATHETER
FDA Adverse Event
Malfunction
·ANGIODYNAMICS·Product code DQO·February 18, 2011
INDURA
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code LKK·February 15, 2008
NUVASIVE COROENT PROCEDURE
FDA Adverse Event
Malfunction
·NUVASIVE, INC.·Product code MQP·April 11, 2013