1,544 results
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33ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Amvex Vacuum Regulator
FDA UDI
OHIO MEDICAL, LLC·00628101501372·VR-PI series, VacReg, Ped Int 3Mode 160mmHg, A...
ambIT PCA*PIB, ambIT PIB, ambIT PIB*PCA, ambIT PIEB, and ambIT Programmable Intermittent Pump
FDA 510(k)
FDA Class 2
·General Hospital
VENT CORP PIB IMPLANT
FDA 510(k)
FDA Class 2
·Dental
MedSource Spine Board
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00840155411807·Pedi Board
ambIT* PIB-PCA Pump
FDA UDI
Avanos Medical, Inc.·00193494000707·PIB-PCA Pump
ambIT* PIB*IL Pump
FDA UDI
Avanos Medical, Inc.·00193494000769·PIB*IL Pump
ambIT* PIB IL v 1.5
FDA UDI
Avanos Medical, Inc.·00193494001384·PIB IL v 1.5
ambIT* KIDS PIB Pump-Blue
FDA UDI
Avanos Medical, Inc.·00193494001216·KIDS PIB Pump-Blue
ambIT* PIB/PCA Pump V1.5
FDA UDI
Avanos Medical, Inc.·00193494001315·PIB-PCA v1.5 Pump
MedSource Immobilization Board
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00816703027776·Pediatric Immobilization Board
MedSource Immobilization Board
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00816703027691·Pedi Board
MedSource Bags
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00816703027714·Pedi Board bag
BioHorizons
FDA UDI
BIOHORIZONS IMPLANT SYSTEMS, INC·00847236016999·Overdenture Lab Process Insert (Black) (4 Pack)
MedSource Immobilization Board
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00816703027707·Pedi Board - Second
Bank-It Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules
FDA UDI
CYTOPHIL, INC.·00852108006312·Synthetic bone graft substitute in particulate ...
MedSource Scoop Stretcher
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00816703026977·Pedi Board
MedSource Immobilization Board
FDA UDI
MEDSOURCE INTERNATIONAL LLC·00816703027790·Pedi Board, Bomberos Logo
Bank-It Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules
FDA UDI
CYTOPHIL, INC.·00852108006329·Synthetic bone graft substitute in particulate ...
Bank-It Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules
FDA UDI
CYTOPHIL, INC.·00852108006305·Synthetic bone graft substitute in particulate ...
PRECISEPLAN 2.15
FDA Adverse Event
Malfunction
·ELEKTA, LTD·Product code MUJ·May 4, 2007