5,129 results · 42ms · Sources: EU EUDAMED, US FDA

Antigen, Cf, T. Cruzi

FDA classification
FDA Class 1 ·Antigen, Cf, T. Cruzi

Liquid Chromatography, Ethosuximide

FDA classification
FDA Class 2 ·Liquid Chromatography, Ethosuximide

ENERPEEL NECK

Basic UDI-DI
EU MDD · Eu Md Class 2a ·GENERAL TOPICS SRL·1 device

AMPUTATION RETRACTOR - COMPRIMETER (CONSISTING OF ARM ANF UPPER THIGHT CUFF, MANOMETER CALIBRATED UPTO 700MM Hg, WITH METEL PUMP)

Basic UDI-DI
EU MDD · Eu Md Class 1 ·Daddy D Pro·1 device

Peak flow meter – Low range 50-300 L/min

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Besmed Health Business Corp.·1 device

Peak flow meter - Standard range 50-800 L/min

Basic UDI-DI
EU MDD · Eu Md Class 2a ·Besmed Health Business Corp.·1 device

OrthAlign Plus

FDA UDI
ORTHALIGN, INC.·00858704006749·Screw, 4.5mm x 25mm, 3.5mm Hex Head

OrthAlign Plus

FDA UDI
ORTHALIGN, INC.·00858704006725·Threaded Fixation Pin, 3.2 mm x 110 mm

OrthAlign Plus

FDA UDI
ORTHALIGN, INC.·00858704006909·Threaded Fixation Pin, 5MM X 170MM

KneeAlign 2

FDA UDI
ORTHALIGN, INC.·00858704006459·Threaded Pin, Headless, 65mm

OrthAlign Plus

FDA UDI
ORTHALIGN, INC.·00851977007352·Threaded Fixation Pin, 3.2mm x 110mm, 0.097 Minor

OrthAlign Plus

FDA UDI
ORTHALIGN, INC.·00858704006640·Screw, 4.5mm x 30mm, 3.5mm Hex Head

OrthAlign Plus

FDA UDI
ORTHALIGN, INC.·00858704006626·Screw, 4.5mm dia x 20mm, 3.5mm Hex Head

Dehydroepiandrosterone sulfate(CLIA)、DHEA-S Calibrators

Basic UDI-DI
EU IVDR · Eu Ivd Class B ·Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·3 devices

Berner Oy

Importer
🇫🇮 Finland·16 Manufacturers

System, Balloon, Intra-Aortic And Control, Reprocessed

FDA classification
FDA Class 3 ·System, Balloon, Intra-Aortic And Control, Reprocessed

Catheter, Oximeter, Fiber Optic, Reprocessed

FDA classification
FDA Class 2 ·Catheter, Oximeter, Fiber Optic, Reprocessed

Trocar, Reprocessed

FDA classification
FDA Class 2 ·Trocar, Reprocessed

Bur, Diamond Coated, Reprocessed

FDA classification
FDA Class 1 ·Bur, Diamond Coated, Reprocessed

Biopsy Device, Percutaneous, Reprocessed

FDA classification
FDA Class 1 ·Biopsy Device, Percutaneous, Reprocessed