64 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STERRAD (R) 100NX DUO CYCLE TEST PACK
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
Smith & Nephew, Inc.·00885556007297·BONE CURETTE CURVED 45 DEG 228.6
...
Bernafon
FDA UDI
Bernafon AG·05711584004432·CT7 CP, VC PS BE CANTEO 7
Medetz Surgical Instruments
FDA UDI
Medetz Surgical Instruments LLC·G2231113910·Braunstein Fixed Caliper 3.5mm & 4.0mm DBL-Ende...
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08800089427949·
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776305048·HEANEY RETR 6.75" MEDIUM 2-78" X 1 18"
MERIT MEDICAL 20 ML SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
SCANDIA-45 GAMMA CAMERA SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022
TOTAL ASR FEM IMP SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·May 14, 2013
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 23, 2014
ASR ACETABULAR CUPS 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 13, 2011
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code HWC·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 40
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 45
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019