17 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MTA2.2 MATERIAL
FDA 510(k)
FDA Class 2
·Dental
VIEWFLEX PLUS ICE CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
EUROIMMUN ANTI-HSV-2 ELISA (IGG) AND ANTI-HSV-1 ELISA (IGG) KIT
FDA 510(k)
FDA Class 2
·Microbiology
BINAX NOW COVID-19 AG CARD
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·December 10, 2021
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
CARDIA DR
FDA Adverse Event
Malfunction
·IPG MFG SWITZERLAND·Product code LWS·October 10, 2014
PRECISION XTRA/OPTIUM
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE INC, USA·Product code NBW·September 10, 2008
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·June 25, 2019
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·June 25, 2019
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·June 26, 2019
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·December 31, 2019
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·December 31, 2019
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·June 14, 2019
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·June 26, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·July 23, 2019
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·August 27, 2019
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026