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)