15 results
·
41ms
·
Sources: EU EUDAMED, US FDA
Auto Disable Syringe
FDA registration
TKMD RWANDA LTD·1 product·🇷🇼 Rwanda
Auto Disable Syringe
FDA 510(k)
FDA Class 2
·General Hospital
Altapore MIS
FDA registration
APATECH LTD.·1 product·🇬🇧 United Kingdom
INNESIS PEEK CAGE
FDA registration
BK MEDITECH, USA·1 product·🇺🇸 United States
Synergy Health Sterilisation UK Ltd
FDA registration
Synergy Health Sterilisation UK Ltd·1 product·🇬🇧 United Kingdom
Altapore MIS
FDA registration
BAXTER HEALTHCARE CORPORATION·1 product·🇺🇸 United States
INNESIS PEEK CAGE
FDA registration
BK MEDITECH CO., LTD.·1 product·🇰🇷 South Korea
HUNT DEVELOPMENTS (UK) LIMITED
FDA registration
HUNT DEVELOPMENTS (UK) LIMITED·1 product·🇬🇧 United Kingdom
DT7308 TENS 7000 Migraine Pain Relief (LT1103)
FDA registration
Shenzhen Dongdixin Technology Co., Ltd.·1 product·🇨🇳 China
DT7308 TENS 7000 Migraine Pain Relief
FDA registration
COMPASS HEALTH BRANDS (CORPORATE OFFICE)·1 product·🇺🇸 United States
INNESIS PEEK CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
RADCALC, MODEL V.4.0
FDA 510(k)
FDA Class 2
·Radiology
Syringe, Piston
FDA classification
FDA Class 2
·Syringe, Piston
Accelerator, Linear, Medical
FDA classification
FDA Class 2
·Accelerator, Linear, Medical
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar