20 results
·
41ms
·
Sources: EU EUDAMED, US FDA
Atellica IM 1600 Analyzer (Refurbished)
FDA registration
Siemens Healthcare Diagnostics Manufacturing Ltd.·3 products·🇮🇪 Ireland
Atellica IM 1600 Analyzer (Refurbished)
FDA registration
SIEMENS HEALTHCARE DIAGNOSTICS INC.·3 products·🇺🇸 United States
Atellica IM 1600 Analyzer (Refurbished)
FDA registration
Siemens Healthcare Diagnostics Inc.·3 products·🇺🇸 United States
Trinidad IM Thyroid Stimulating Hormone (TSH) Assay, Trinidad IM TSH Calibrators, Trinidad Immunoassay (IM) System
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100240·SILICONE TUBING FOR ASPIRATING SPECULUM
Eurofins STERIPAC GMBH
FDA registration
Eurofins STERIPAC GMBH·2 products·🇩🇪 Germany
MOBIS PEEK
FDA registration
PROCON MEDIZINTECHNIK GMBH·2 products·🇩🇪 Germany
NeuViz 64 In, NeuViz 64 En
FDA registration
NEUSOFT MEDICAL SYSTEMS CO., LTD.·1 product·🇨🇳 China
Synergy Health Allershausen GmbH
FDA registration
Synergy Health Allershausen GmbH·2 products·🇩🇪 Germany
MOBIS XL SPINAL IMPLANT SYSTEM
FDA registration
SIGNUS MEDIZINTECHNIK GMBH·2 products·🇩🇪 Germany
Synergy Health Daniken AG
FDA registration
Synergy Health Daniken AG·2 products·🇨🇭 Switzerland
Radioimmunoassay, Thyroid-Stimulating Hormone
FDA classification
FDA Class 2
·Radioimmunoassay, Thyroid-Stimulating Hormone
SYNTHECEL DURA REPAIR, SYNTHECEL DURA ONLAY
FDA registration
Synthes (USA) Products LLC·1 product·🇺🇸 United States
ID NOW Influenza A & B 2
FDA registration
ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·3 products·🇺🇸 United States
EliA IgG/IgM/IgA Negative Control 2500/5000
FDA registration
PHADIA AB·2 products·🇸🇪 Sweden
Synthecel Dura Repair, Synthecel Dura Onlay
FDA registration
SYNTHES GMBH·1 product·🇨🇭 Switzerland
LIV LINDE INTERGRATED VALVE-PORTABLE OXYGEN SYSTEM, MODEL M706
FDA 510(k)
FDA Class 1
·Anesthesiology
MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI
FDA 510(k)
FDA Class 2
·Orthopedic
Cylinder, Compressed Gas, And Valve
FDA classification
FDA Class 1
·Cylinder, Compressed Gas, And Valve
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar