26 results · 20ms · Sources: EU EUDAMED, US FDA

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RenovoCath

FDA 510(k)
FDA Class 2 ·Cardiovascular

Audina

FDA UDI
Bernafon AG·05711584086407·CAPTO 5 B 105, 2.4G NFM DPB MSIL AUDIN

OneLIF™

FDA UDI
Novapproach Spine LLC·G07001131916060·Trial-OneLIF Interbody, Large, 19 Degree, 16mm ...

OneLIF™

FDA UDI
Novapproach Spine LLC·G07001031916060·OneLIF Interbody, Large, 19 Degree, 16mm X 6mm

Vacutron

FDA UDI
Allied Medical, LLC·00026072010730·Mini-Vac

VERTAPLEX HV (SINGLE PACK AND DUAL PACK)

FDA 510(k)
FDA Class 2 ·Orthopedic

MICROMED PD-8K INSULATION DEFECT DETECTOR

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2020

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076331591·Rasp, 19x16mm, 6mm height, 6-degree

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076336015·Trial, 19x16mm, 6mm height, 12-degree

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076330945·Trial, 19x16mm, 6mm height,

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076330259·3D Porous Titanium Cervical Interbody, 19x16mm,...

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076336855·Rasp, 19x16mm, 6mm height, 12-degree stopless

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076331263·Trial, 19x16mm, 6mm height, 6-degree

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076336299·Rasp, 19x16mm, 6mm height, 12-degree

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076335735·3D Porous Titanium Cervical Interbody, 19x16mm,...

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076330570·3D Porous Titanium Cervical Interbody, 19x16mm,...

Flux-C Cervical Interbody

FDA UDI
Ulrich Medical Usa, Inc.·00810076336572·Trial, 19x16mm, 6mm height, 12-degree stopless

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 22, 2014

DEPUY ASR XL FEM IMP SIZE 49

FDA Adverse Event
Injury ·DEPUY INTL., LTD. - 8010379·Product code KXA·June 26, 2013