20 results · 45ms · Sources: EU EUDAMED, US FDA

SpyGlass DS Digital Controller

FDA registration
ENERCON TECHNOLOGIES·3 products·🇺🇸 United States

SpyGlass DS Direct Visualization System

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Choledochoscope And Accessories, Flexible/Rigid

FDA classification
FDA Class 2 ·Choledochoscope And Accessories, Flexible/Rigid

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814190·GENUMEDI PT SILVER L II

HardyCHROM MRSA

FDA registration
Hardy Diagnostics·1 product·🇺🇸 United States

Venture Cervical Plate

FDA registration
WARSAW ORTHOPEDIC, INC.·1 product·🇺🇸 United States

HardyCHROM MRSA

FDA registration
HARDY DIAGNOSTICS·1 product·🇺🇸 United States

Venture Cervical Plate

FDA registration
Medtronic Medical Costa Rica S.R.L.·1 product·🇨🇷 Costa Rica

Venture Cervical Plate

FDA registration
Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

Venture Cervical Plate

FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

Venture Cervical Plate

FDA registration
MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·1 product·🇺🇸 United States

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00840180523254·DIAGONAL CORNER DRILL GUIDE - THREAD IN, 22MM

cobas 4800 Cdiff Amplification/Detection Kit, 240 Tests

FDA registration
ROCHE DIAGNOSTICS GMBH·2 products·🇩🇪 Germany

Medline ReNewal

FDA registration
Medline ReNewal·1 product·🇺🇸 United States

Merits Yoga Power Scooter, S542

FDA registration
MERITS HEALTH PRODUCTS CO., LTD.·1 product·🇹🇼 Taiwan

HARDYCHROM MRSA

FDA 510(k)
FDA Class 2 ·Microbiology

VENTURE ANTERIOR CERVICAL PLATING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Gentuity HF-OCT Imaging System

FDA UDI
GENTUITY LLC·00859910007032·Gentuity OCT imaging console, including optical...

Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar

FDA classification
FDA Class 2 ·Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar

Appliance, Fixation, Spinal Intervertebral Body

FDA classification
FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body