5,129 results
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42ms
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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
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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