22 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Valeo II Interbody Fusion Device System
FDA 510(k)
FDA Class 2
·Orthopedic
Accufuse Cervical System
FDA UDI
ABSOLUTE ADVANTAGE MEDICAL, LLC·00810016801290·Cervical Peek 16mmx14mmx5mm 7° Lordosis
LoFric® Sense™
FDA UDI
Wellspect AB·07333387023182·Single Use Urinary Catheter with salt solution....
LoFric® Sense™
FDA UDI
Wellspect AB·07392532086489·Single Use Urinary Catheter with salt solution....
Ti3D CERVICAL
FDA UDI
XENIX MEDICAL LLC·00818345020917·CERVICAL CAGE 16W x 14D x5H, 6 DEG
McKesson
FDA UDI
MCKESSON MEDICAL-SURGICAL INC.·20612479223732·Transducer Cover
BD BBL¿ TRYPTICASE SOY AGAR WITH 5% SHEEP BLOOD (TSA II)
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·August 30, 2021
APNEALINK, MODEL 22302
FDA 510(k)
FDA Class 2
·Anesthesiology
BEVER UNOCATED / COATED, PAEDIATRIC / MALE / FEMALE NELATON-TIP / TIEMANN-TIP INTERMITTENT CATHETER,
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331171·Trial, 16x14mm, 5mm height, 6-degree
ShurFit ACIF 2C
FDA UDI
PRECISION SPINE, INC.·00840019921299·ACIF Trial, 16 x 14 x 5
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330167·3D Porous Titanium Cervical Interbody, 16x14mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330488·3D Porous Titanium Cervical Interbody, 16x14mm,...
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076331508·Rasp, 16x14mm, 5mm height, 6-degree
Flux-C Cervical Interbody
FDA UDI
Ulrich Medical Usa, Inc.·00810076330853·Trial, 16x14mm, 5mm height,
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·June 11, 2013
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011
SILICONE ADVANCED OPTIC-VIOLET SHIELD
FDA Adverse Event
Malfunction
·BAUSCH & LOMB·Product code HQL·September 12, 2008
CROSSER CATHETER 14S
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code PDU·March 29, 2017
CROSSER CATHETER 14S
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code PDU·March 29, 2017