27 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PALAMED
FDA 510(k)
FDA Class 2
·Orthopedic
Hi-Torque Proceed™
FDA UDI
ABBOTT VASCULAR INC.·08717648321382·Hi-Torque Proceed 220T Angled Guide Wire w/Hydr...
Graves Speculum X Large
FDA UDI
MEDGYN PRODUCTS, INC.·M803030904·Graves Speculum X Large 1 1/2" x 6 1/2" (38mm ...
LEONE SPA
FDA UDI
LEONE SPA·08033707065715·INTRAORAL ELASTICS 4,5 oz 5/16" blue
Ventilator
FDA UDI
Zoll Medical Corporation·00847946024130·CLAMP WITH DOVETAIL,CCLAW
LINEAR ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 10, 2019
PENADAPT 10
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
General Instruments
FDA UDI
ORTHOPEDIATRICS CORP.·00841132132463·SEAT POST CAP - LONG
General Instruments
FDA UDI
ORTHOPEDIATRICS CORP.·00841132150573·Seat, Split
Spica Table
FDA UDI
ORTHOPEDIATRICS CORP.·00841132135174·OP REPACKAGE BASE
RADIANALYZER¿ XPRESS¿
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.·Product code DQK·November 17, 2017
8030904-1997-90002
FDA Adverse Event
Injury
·Product code DXC·September 16, 1997
8030904-1997-90001
FDA Adverse Event
Product code DXC·September 16, 1997
8030904-2005-00001
FDA Adverse Event
Injury
·RADI MEDICAL SYSTEMS AB·Product code DQX·August 26, 2005
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·June 22, 2017
ASSURITY MRI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·December 7, 2022
HELICAL BLADE INSERTER
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code LXH·April 2, 2013
SEBRA SEALER 2380 AND SEBRA SEALER HEAD 1105
FDA Adverse Event
Injury
·HAEMONETICS CORP.·Product code GKT·March 21, 2011
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008