21 results · 43ms · Sources: EU EUDAMED, US FDA

Sterigenics US LLC

FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States

LISI MEDICAL Remmele

FDA registration
LISI MEDICAL Remmele·1 product·🇺🇸 United States

ASFORA BULLET CAGE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Prometey

FDA registration
Spectrum International, Inc.·1 product·🇺🇸 United States

ISOMEDIX OPERATIONS INC.

FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

BS-2

FDA registration
TOCHIGICHIZUKA PLANT·2 products·🇯🇵 Japan

BS-2 Balloon for DBE

FDA registration
FUJIFILM Healthcare Manufacturing Corporation Sano Office·2 products·🇯🇵 Japan

RegenKit - THT

FDA registration
Regenlab USA LLC·1 product·🇺🇸 United States

STRYKER EMEA Supply Chain Services

FDA registration
STRYKER EMEA Supply Chain Services·1 product·🇳🇱 Netherlands

BS-2 Balloon for DBE

FDA registration
FUJIFILM CORPORATION·2 products·🇯🇵 Japan

RegenKit - THT

FDA registration
REGEN LAB Sa·1 product·🇨🇭 Switzerland

Synergy Health Daniken AG

FDA registration
Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

Single Use Surgical Optical Fiber

FDA UDI
QUANTA SYSTEM SPA·08033945937232·Single Use Surgical Optical Fiber ø 200 µm Dist...

3-LD Set, SNAP to DIN, UNSHIELDED, A,48"

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828147101·3-LD Set, SNAP to DIN, UNSHIELDED, A,48"

Vermed

FDA UDI
GRAPHIC CONTROLS ACQUISITION CORP·00009336008339·Din Lead Wire, Snap to Socket, 48", White

COOK INCORPORATED

FDA registration
COOK INCORPORATED·1 product·🇺🇸 United States

M2376A DEVICELINK SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1

FDA 510(k)
FDA Class 2 ·General Hospital

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification
FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)