38 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NC EUPHORA RAPID EXCHANGE BALLOON DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Kirwan
FDA UDI
KIRWAN SURGICAL PRODUCTS LLC·00841019103531·Disposable Bipolar Forceps Non-Stick 4" (10.2cm...
Portex
FDA UDI
ICU MEDICAL, INC.·15019315019753·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197538190·Killian Nasal Speculum
90mm, ...
EASYRA ALKALINE PHOSPHATASE, ASPARTATE AMINOTRANSFERASE AND AMYLASE REAGENTS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
HDL-EX SEIKEN ASSAY KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·October 3, 2014
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 24, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 27, 2011
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·April 28, 2020
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·April 11, 2017
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·February 11, 2020
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·January 19, 2023
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 12, 2019