245 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KIMGUARD ONE STEP STERILIZATION WRAP
FDA 510(k)
FDA Class 2
·General Hospital
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304232624·
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221037930·Unitek(TM) Bicuspid Band General Purpose Wide U...
HAcancellous™ PEEK-C
FDA UDI
INNO Holdings, Inc.·M711591417120·HAcancellous PEEK-C, 14L x 17W x 12H x 8°, HA P...
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321417120·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311417120·
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071147419·14F x 1.7cm MiniSPC Low Profile Suprapubic Cath...
K2M General Instruments
FDA UDI
VB Spine LLC·10888857583184·Modular Trial 22x8x17mm, 7°
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011141712000·Polishing brush for polishing machines, 3 numbe...
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071150037·14F x 1.7cm MiniSPC Low Profile Suprapubic Cath...
ENDOVASCULAR LAER VEIN SYSTEM KIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
'RAPIDTEC 4' TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 4, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
JOURNEY GUIDEWIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·June 27, 2011
COOK CELECT PLATINUM NAVALIGN JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·September 12, 2019
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·January 29, 2020
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·March 31, 2020
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·September 19, 2019
GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·February 23, 2022