23 results
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44ms
·
Sources: EU EUDAMED, US FDA
PowerPort with Groshong Catheter
FDA registration
C.R. BARD, INC.·1 product·🇺🇸 United States
PowerPort with Groshong Catheter
FDA registration
BARD REYNOSA S.A. DE C.V.·1 product·🇲🇽 Mexico
PowerPort with Groshong Catheter
FDA registration
C.R. BARD, INC.·1 product·🇺🇸 United States
PowerPort with Groshong Catheter
FDA registration
Bard Access Systems, Inc.·1 product·🇺🇸 United States
MALLEABLE TUNNELER, SINGLE BARB, 8 FR
FDA registration
TURNXON PRECISION CO., LTD·1 product·🇨🇳 China
POWERPORT IMPLANTED PORT WITH GROSHONG CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
SYNTHES (USA) ORIBITAL MESH PLATES
FDA registration
EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States
SYNTHES (USA) ORIBITAL MESH PLATES
FDA registration
Synthes (USA) Products LLC·1 product·🇺🇸 United States
Plate, fixation, bone
FDA registration
SYNTHES GMBH·1 product·🇨🇭 Switzerland
Jabil Inc. (Monument)
FDA registration
Jabil Inc. (Monument)·1 product·🇺🇸 United States
TECOMET
FDA registration
TECOMET·1 product·🇺🇸 United States
Synthetic absorbable seeding spacer
FDA registration
THERAGENICS CORP.·1 product·🇺🇸 United States
BioSpacer 910; Accu-Space
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Specials
FDA UDI
SEASPINE ORTHOPEDICS CORPORATION·10889981291242·Trial Rasp, 14 x 13 x 11mm, 7° Lordosis
Port & Catheter, Implanted, Subcutaneous, Intravascular
FDA classification
FDA Class 2
·Port & Catheter, Implanted, Subcutaneous, Intravascular
VITROS Na+ Slides
FDA registration
ORTHO-CLINICAL DIAGNOSTICS, INC.·2 products·🇺🇸 United States
LEGION
FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States
VITROS Na+ Slides
FDA registration
ORTHO-CLINICAL DIAGNOSTICS, INC.·2 products·🇺🇸 United States
VITROS Na+ Slides
FDA registration
Ortho-Clinical Diagnostics European Support Center·2 products·🇫🇷 France
SYNTHES (USA) ORIBITAL MESH PLATES
FDA 510(k)
FDA Class 2
·Orthopedic