20 results
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41ms
·
Sources: EU EUDAMED, US FDA
Alkaline Phosphatase (TRIS)
FDA registration
Fisher Diagnostics·1 product·🇺🇸 United States
ALP (ALKALINE PHOSPHATASE) REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes
FDA classification
FDA Class 2
·Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes
Surgical Face Masks（MEDLINE ADMIN KITS）
FDA registration
XIANNING ECO MEDICAL ARTICLES CO., LTD.·1 product·🇨🇳 China
DISPOSABLE MASK
FDA registration
XIANNING ECO MEDICAL ARTICLES CO., LTD.·1 product·🇨🇳 China
Medline Surgical Face Mask and Medline Procedural Face Mask
FDA registration
XIANNING ECO MEDICAL ARTICLES CO., LTD.·1 product·🇨🇳 China
COVERALL
FDA registration
XIANNING ECO MEDICAL ARTICLES CO., LTD.·1 product·🇨🇳 China
DISPOSABLE SURGICALBOUFFANT CAP
FDA registration
XIANNING ECO MEDICAL ARTICLES CO., LTD.·1 product·🇨🇳 China
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471159419·SAGITTAL BLADE - DE SOUTTER STANDARD 5.5 x 35 x...
ISOMEDIX OPERATIONS INC.
FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States
MICROPORT ORTHOPEDICS INC.
FDA registration
MICROPORT ORTHOPEDICS INC.·1 product·🇺🇸 United States
Isomedix Operations, Inc.
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
ISOMEDIX OPERATIONS INC.
FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States
ISOMEDIX OPERATIONS INC.
FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States
PL Tubing Set (STERILE)
FDA registration
Engineered Medical Systems, LLC·1 product·🇺🇸 United States
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837012434·
MODIFICATION TO: CARDIMA ABLATION SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AccuLIF TL and PL Cage
FDA 510(k)
FDA Class 2
·Orthopedic
Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
FDA classification
FDA Class 2
·Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar