28 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RENEW NEUROSTIMULATION SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741155284·Catheter Placement Kit
Implant Prosthetics
FDA UDI
Preat Corporation·00842092118252·NobelActive™/Conical-compatible NP Titanium .05...
Precisor
FDA UDI
Conmed Corporation·20653405051906·Precisor Hot Disposable Hot Biopsy Forceps, 2.3...
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 12, 2024
X-RAY MONOBLOCK, MONOBLOCK XRS-60-330
FDA 510(k)
FDA Class 1
·Radiology
KIPPMED I.V. MANIFOLD
FDA 510(k)
FDA Class 2
·General Hospital
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 12, 2024
NA
FDA UDI
Zimmer, Inc.·00889024024366·
NA
FDA UDI
Zimmer, Inc.·00889024024359·
NA
FDA UDI
Zimmer, Inc.·00889024024380·
NA
FDA UDI
Zimmer, Inc.·00889024024373·
NA
FDA UDI
Zimmer, Inc.·00889024024397·
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 12, 2024
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC·Product code NBW·December 27, 2016
VERSAFITCUP CC TRIO 01.26.3239HCT FLAT PE HC LINER Ø 32 / C
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·February 11, 2022
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013
EON RECHARGEABLE IPG
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 17, 2011
LIFESHIELD FILTER SOLUSET
FDA Adverse Event
Malfunction
·HOSPIRA DE COSTA RICA LTD.·Product code FPB·February 18, 2008
Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.
FDA Enforcement
Class II
·Terminated·Myolyn Inc.·August 24, 2022