49 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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URSA ANGIOGRAPHIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Portex
FDA UDI
ICU MEDICAL, INC.·20351688017199·
Novo Surgical Inc.
FDA UDI
NOVO SURGICAL, INC.·00842331131707·knife handle #7, for blades 10-15c, 6 1/2" (16....
Bausch & Lomb Incorporated
FDA registration
Bausch & Lomb Incorporated·5 products·🇺🇸 United States
CASCADIA™ Interbody System
FDA UDI
VB Spine LLC·10888857554726·Trial Size 16x20x13 mm, Convex
FIBERFILL AGP
FDA 510(k)
FDA Class 2
·Dental
CONFIRM ANTI-PROGESTORONE RECEPTOR (1E2) RABBIT MONOCLONAL PRIMARY ANTIBODY
FDA 510(k)
FDA Class 2
·Hematology
INCLUSIVE TAPERED IMPLANT 5.2 MMD X 8 MML X 4.5 MMP
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·December 12, 2023
DUO FLUID CART
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·December 21, 2017
ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·August 31, 2018
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 22, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code FKX·September 26, 2014
PREVA DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·June 14, 2011
PROSOUND F75 ULTRASOUND SCANNER
FDA Adverse Event
Malfunction
·HITACHI ALOKA MEDICAL, LTD·Product code GXX·July 16, 2014
ULTRAFLEX DUO HIGH FLUID CART - REFURBISHED
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·June 25, 2020
EVAC STATION
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·September 5, 2017
ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·January 11, 2018
EVAC STATION
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·January 16, 2018
ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·June 7, 2018
ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR
FDA Adverse Event
Malfunction
·DORNOCH·Product code JCX·August 3, 2017