39 results · 26ms · Sources: EU EUDAMED, US FDA

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MEGA 2000 SOFT DUAL CORD PATIENT RETURN ELECTRODE PAD

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

RELISA MPO-ANCA TEST SYSTEM FOR ANTIBODIES TO MYELOPEROXIDASE, MODEL # 7096-15

FDA 510(k)
FDA Class 2 ·Immunology

AMMONIA-L3K ASSAY, MODEL 263-17, AMMONIA-L3K ASSAY, MODEL 263-30

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

SAFIL VIOLET 8/0 (0.4) 30CM 2XDLM6

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·August 9, 2019

ULTRA DRIVE 6MM PLUG PULLER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDX·July 20, 2022

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 27, 2017

TSRH

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 12, 2017

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code NIQ·April 2, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·March 16, 2011

SERVO-S

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·March 27, 2008

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 2, 2018

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·June 21, 2011

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·June 21, 2011

TSRH

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 29, 2016

TSRH

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 29, 2016

SAFIL VIOLET 1 (4) 90CM HR48 (M)

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·November 20, 2019

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·March 25, 2011

SAFIL UNDYED 4/0 (1,5) 45CM DS19 (M)

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·July 5, 2019