2,730 results · 22ms · Sources: EU EUDAMED, US FDA

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VALIANT STENT GRAFT

FDA Adverse Event
Death ·MEDTRONIC IRELAND·Product code MIH·January 29, 2020

VALIANT STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·January 29, 2020

V MUELLER BE 2847

FDA Adverse Event
Other ·ALLEGIANCE HEALTHCARE CORP.·Product code KAK·April 4, 2000

JAKO LARYNGEAL PROBE, ANGLED

FDA Adverse Event
Malfunction ·Product code KAK·April 28, 2000

STORZ

FDA Adverse Event
Injury ·STORZ·Product code KAK·August 11, 2023

ENLO FLO SUCTION IRRIGATOR PROBE

FDA Adverse Event
Malfunction ·DAVOL, INC.·Product code KAK·August 11, 1994

MAXILLARY OSTIOUM SEEKER PROBE

FDA Adverse Event
Malfunction ·EXPLORENT CHIRURGISCHE INSTRUMENTE GMBH·Product code KAK·May 17, 2017

PILLING WECK

FDA Adverse Event
Malfunction ·PILLING WECK SURGICAL SURGICAL DIVISION·Product code KAK·November 19, 1998

STORZ

FDA Adverse Event
Other ·STORZ INSTRUMENT CO·Product code KAK·February 10, 1999

Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature

FDA Recall
Terminated ·Vital Signs Colorado Inc.·Product code KAK·August 17, 2012

Probe, Ent

FDA classification
FDA Class 1 ·Probe, Ent

AMII AMERICA KIT

FDA UDI
InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)·08809986680235·

Endo Access

FDA UDI
TULSA DENTAL PRODUCTS LLC·D716EAK1·Endo Access Kit - Holder & Ins

MARCHON JAPAN K.K.

FDA registration
MARCHON JAPAN K.K.·3 products·🇯🇵 Japan

KOBAYASHI SHOJI K.K.

FDA registration
KOBAYASHI SHOJI K.K.·5 products·🇯🇵 Japan

Cardinal Health K.K.

FDA registration
Cardinal Health K.K.·10 products·🇯🇵 Japan

KATO KOGEI,K.K

FDA registration
KATO KOGEI,K.K·2 products·🇯🇵 Japan

INFELD OPTICA K.K

FDA registration
INFELD OPTICA K.K·2 products·🇯🇵 Japan

HOSHIDEN WAKAYAMA K.K.

FDA registration
HOSHIDEN WAKAYAMA K.K.·1 product·🇯🇵 Japan

BAK®

FDA UDI
ZIMMER SPINE, INC.·00889024333192·