20 results
·
33ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ICEROD CX CRYOABLATION NEEDLE ICEROD CX CRYOABLATION NEEDLE MULTIPACK
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813148·GENUMEDI PRO SILVER SIZE I
ArgenZ Anterior 95x10 #3
FDA UDI
ARGEN CORPORATION, THE·D818121251·Dental porcelain/ceramic restoration kit
SPROTTE®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223107478·Distal Tip: SPROTTE®
Proximal End: ISO 80369-7
SPROTTE®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223116227·Needle
SPROTTE®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223107461·Distal Tip: SPROTTE®
Proximal End: ISO 80369-7
SPROTTE®
FDA UDI
Pajunk GmbH Medizintechnologie·04048223116210·Needle
SPROTTE® 2.G
FDA UDI
Pajunk GmbH Medizintechnologie·14048223024376·SPROTTE® 2.G
Standa...
SPROTTE® 2.G
FDA UDI
Pajunk GmbH Medizintechnologie·14048223022808·SPROTTE® 2.G
Standa...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450835777·
IMMUNOCAP ALLERGEN D202, ALLERGEN COMPONENT NDER P 1, HOUSE DUST MITE, IMMUNOCAP ALLERGEN D203, ALLERGEN
FDA 510(k)
FDA Class 2
·Immunology
ST/AR ST AND ARRHYTHMIA SOFTWARE, RELEASE E.I.
FDA 510(k)
FDA Class 2
·Cardiovascular
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970423·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970393·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970416·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970409·
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 21, 2024
IDENTITY XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 13, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
AML 10.5 MMA 6.3 5/8 STD 12/14
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 1, 2011