122 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WARMTOUCH CARDIAC BLANKET,CATALOG # 503-0860
FDA 510(k)
FDA Class 2
·Cardiovascular
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00141211·
Tandem Mobi Autosoft 30 Kit
FDA UDI
Tandem Diabetes Care, Inc.·00389152412177·Autosoft 30, 23"/13mm, 10 pack kit
Baby Gorilla/Gorilla Plating System
FDA UDI
Paragon 28, Inc.·00889795009197·Gorilla, Plate, 28-Plate, 4 Hole Locking, Small...
ADVIA® Chemistry ALB Albumin BCG Reagents
FDA UDI
Siemens Healthcare Diagnostics Inc.·00630414209586·Albumin - ADVIA Chem. - RGT - 4x555/4x232 tests
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563762·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563786·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563816·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563830·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563779·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563823·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563809·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563793·
RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS
FDA 510(k)
FDA Unclassified
·Unknown
STERILE BUTTON PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
THERMACHOICE CATHETER UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code MNB·December 7, 2018
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
QUICKSITE LV
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·March 10, 2011
VISION ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·March 13, 2008
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026