29 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDRANGE ELECTROSURGICAL EXPANSION SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ArgenZ HT+ 98x25 A1-L
FDA UDI
ARGEN CORPORATION, THE·D818122092·Dental porcelain/ceramic restoration kit
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973134·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970461·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970454·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973615·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973608·
Monobloc K-Wire Inserter 3.2mm
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215075842·
K wire 220mm
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215075828·The saleable unit (device count) is 1, there ar...
K wire 220mm
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215075835·The saleable unit (device count) is 1, there ar...
Monobloc K-Wire Inserter 4.5mm
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215075859·
Monobloc K-Wire Inserter Big Daddy
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039523·
PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNTEX PRE-POWDERED LATEX EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
GMK-PRIMARY FEMUR STD CEMENTED SIZE 3
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·December 16, 2022
THORATEC VENTRICULAR ASSIST DEVICE (VAD) SYSTEM
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·May 16, 2013
EXPEDIUM OR MOSS MIAMI SCREW
FDA Adverse Event
Injury
·DEPUY SYNTHES SPINE·Product code NKB·September 26, 2014
SELECTOR CONSOLE 120V WITH FOOTSWITCH
FDA Adverse Event
Malfunction
·INTEGRA, ANDOVER·Product code LFL·May 24, 2011
COOK TURBO-FLO HD HEMODIALYSIS CATHETER SET
FDA Adverse Event
Injury
·COOK INC·Product code MPB·February 13, 2017
INSTINCT JAVA SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MNH·October 30, 2019