16 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SILASTIC BRAND FOLEY CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Lumbar Catheter
FDA UDI
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)·10381780034247·The Integra Y- Lumbar Catheter consists of a F5...
Steri Irrigation Tip
FDA UDI
DiaDent Group International·08806383562454·Steri Irrigation Tip Side Open Type designed as...
HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORY
FDA 510(k)
FDA Class 2
·Ophthalmic
ASAHI Corsair Microcatheter
FDA 510(k)
FDA Class 2
·Cardiovascular
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·February 8, 2013
BIOMET
FDA Adverse Event
Injury
·Product code KWA·December 29, 2010
V200 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC.·Product code CBK·July 22, 2014
AIA-900
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·February 24, 2016
8100 ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 10, 2021
ACIST
FDA Adverse Event
Malfunction
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007
TOSOH AIA-900
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·December 13, 2016
A1A-600II
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·October 28, 2016
TOSOH AIA-1800
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·November 11, 2016
AIA-360
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·March 3, 2016
Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024