4,678 results · 25ms · Sources: EU EUDAMED, US FDA

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SMOOV O10

FDA 510(k)
FDA Class 2 ·Physical Medicine

Echo® Bi-Metric® Hip System

FDA UDI
Biomet Orthopedics, LLC·00887868260476·

ECHO BI-METRIC HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304463394·

Bernafon

FDA UDI
Bernafon AG·05711584086902·ZR3, KIT 312 NFM 90 PB R BE ZERENA 3

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776199876·LLETZ PEDS SPEC L ET

OsteoMed

FDA UDI
OSTEOMED LLC·00845694009614·2.0mm x 16mm Cannulated Lag Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694070225·Cannulated 2.0 x 16mm Lag Screw Sterile Qty 5

SUPER-FINE PEN NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

PRECICONTROL CLINCHEM MULTI 1 AND 2

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

UNKNOWN DEPUY INSERT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 6, 2008

DUROM HIP GENERIC

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·June 20, 2013

RF3000 RADIOFREQUENCY GENERATOR

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·August 4, 2011

COCHLEAR BAHA CONNECT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·September 18, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·November 11, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·September 13, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 2, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·September 16, 2016

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·August 15, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·June 1, 2016

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·October 13, 2016