4,866 results · 41ms · Sources: EU EUDAMED, US FDA

Accessories, Soft Lens Products

FDA Pre-Market Approval
FDA Class 2 ·CIBA VISION LENS DROPS

Powder-Free Polychloroprene Patient Examination Glove

FDA classification
FDA Class 1 ·Powder-Free Polychloroprene Patient Examination Glove

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

Surgeon'S Gloves

FDA classification
FDA Class 1 ·Surgeon'S Gloves

CQI ABO-D - RH.K - CONTRÔLE QUALITÉ INTERNE POUR LA DÉTERMINATION DES GROUPES SANGUINS DANS LES SYSTÈMES ABO RHÉSUS KELL- BLISTER (EFS)

Basic UDI-DI
EU IVDD · Eu Ivd Annex 2 List A ·ETABLISSEMENT FRANCAIS DU SANG·1 device

CQI ABO-D - Rh.K - Contrôle Qualité Interne pour la détermination des groupes sanguins dans les systèmes ABO Rhésus Kell - Blister (grifols)

Basic UDI-DI
EU IVDD · Eu Ivd Annex 2 List A ·ETABLISSEMENT FRANCAIS DU SANG·1 device

Disposable Membrane Oxygenator

Basic UDI-DI
EU MDR · Eu Md Class 2a ·CHINABRIDGE (SHENZHEN) MEDICAL TECHNOLOGY CO., LTD.·2 devices

Flow Cytometric Test System For Hematopoietic Neoplasms

FDA classification
FDA Class 2 ·Flow Cytometric Test System For Hematopoietic Neoplasms

Reservoir, Blood, Cardiopulmonary Bypass, Exempt

FDA classification
FDA Class 2 ·Reservoir, Blood, Cardiopulmonary Bypass, Exempt

Piccolo MetLyte Plus CRP

FDA UDI
ABAXIS, INC.·EABA40000341·The Piccolo® MetLyte Plus CRP reagent disc, use...

Non-Niosh-Approved Disposable Filtering Facepiece Respirators (Ffrs)

FDA classification
FDA Not Classified ·Non-Niosh-Approved Disposable Filtering Facepiece Respirators (Ffrs)

EF LINE

Basic UDI-DI
EU MDR · Eu Md Class 1 ·ORTHOPLUS·85 devices

MediMark Europe Sarl.

Authorized representative
🇫🇷 France·35 Manufacturers·3394 Devices

Medikon Sağlık Turizm Seyahat Dan. Hiz. İth. İhr. ve Tic. Ltd. Şti.

Importer
🇹🇷 Türkiye