10,000 results
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47ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Anchor Drill
FDA UDI
ARUM DENTISTRY Co., Ltd.·08800265649547·
KRONUS GAD AUTOANTIBODY ELISA ASSAY KIT
FDA 510(k)
FDA Class 2
·Immunology
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094269871·ELI150c 12-Lead Multi-Channel Electrocardiograp...
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094302721·ELI150c 12-Lead Multi-Channel Electrocardiograp...
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094269864·ELI150c 12-Lead Multi-Channel Electrocardiograp...
BK-5371 GAD-19-BOUT PERSONAL MOBIL AID
FDA 510(k)
FDA Class 1
·Physical Medicine
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SAS·Product code HAW·February 28, 2022
BLOOD GADS, ELECTROLYTE, GLUCOSE, LATATE AND BUN QUALITY CONTROL PRODUCT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
NEUROBLATE® SYSTEM
FDA Adverse Event
Malfunction
·MONTERIS MEDICAL CORPORATION·Product code GEX·October 31, 2016
PROCLAIM 7 ELITE IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·March 19, 2021
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·October 21, 2010
MARK V PROVIS
FDA Adverse Event
MEDRAD, INC.·Product code IZQ·July 21, 2009
ELITE, ROLL AROUND INJ SYSTEM
FDA Adverse Event
Malfunction
·LIEBEL-FLARSHEIM·Product code DXT·August 24, 2021
INNER SHEATH, FOR 26 FR. OUTER SHEATH
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HIH·January 21, 2026
ETHISORB DURA-PATCH
FDA Adverse Event
Injury
·ETHICON INC.·Product code GXQ·April 17, 2023
ANYPLUS
FDA Adverse Event
Injury
·Product code MAX·December 20, 2019
ENDOWRIST
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·March 2, 2026
MORCELLATION
FDA Adverse Event
Injury
·Product code HET·October 2, 2014
OPTISTAR LE, INJECTOR SYSTEM
FDA Adverse Event
Injury
·LIEBEL-FLARSHEIM CO.·Product code DXT·May 1, 2009
OBSIDIO
FDA Adverse Event
Malfunction
·OBSIDIO, INC.·Product code KRD·November 25, 2025