30 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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H.M.T. ACUPUNCTURE NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
n/a
FDA UDI
Ortho Development Corporation·00822409072521·Blunt Tip Broach Size 1
ICU Medical
FDA UDI
ICU MEDICAL, INC.·00840619023348·ChemoClave™ Vented Vial Spike
Minute Stain - L.M.D. Elixirs
FDA UDI
Taub Products·D8370125010·Minute Stain's Larry’s Magical Denture Elixirs ...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993137336·CUSTOM SEAMLESS SOFT 3/AG-HT ONE LEG PANTY/CLOS...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993131815·CUSTOM SEAMLESS SOFT 1/AG-HT ONE LEG PANTY/CLOS...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993139521·CUSTOM SEAMLESS SOFT 2/AG-HT ONE LEG PANTY/CLOS...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694012294·Single Silicone Tubing Set, 12 ft. (Clips Inclu...
Phonak
FDA UDI
Phonak AG·07613275044933·Phonak Dalia 13 UZ Petite
SMARTSCREW
FDA 510(k)
FDA Class 2
·Orthopedic
ENDOPOUCH RETRIEVER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180503683·Tip, Curette, Cup, Size 2, Straight, Smooth
VIDAS Clostridium Difficile GDH, REF 30125-01
FDA Recall
Open, Classified
·bioMerieux, Inc.·Product code MCB·September 22, 2021
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·March 20, 2013
S4S/SUR-FIT NATURA 2 PC - 2 PC DURAHESIVE (DH)
FDA Adverse Event
Injury
·CONVATEC INC.·Product code EXE·August 12, 2014
HIGH PRESSURE TUBING IN A CUSTOM KIT
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code BYX·March 12, 2008
VIDAS Clostridium Difficile GDH, REF 30125-01
FDA Enforcement
Class II
·Ongoing·bioMerieux, Inc.·January 5, 2022
PREMICRON GREEN 4/0(1,5)4X45 HR13 TOM
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAT·January 29, 2020
BD DISCARDIT¿ II SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 9, 2022
PREMICRON GREEN 2/0 (3) 75CM HR26 (M)
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAW·June 28, 2019