33 results
·
44ms
·
Sources: EU EUDAMED, US FDA
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077120·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077090·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304077106·
neoWave LS
FDA UDI
Ht Medical, LLC·00818345023888·BAYONETTED PUSH SCRAPER CURETTE
Reprocessed Electric Biopsy Forceps
FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States
Reprocessed Electric Biopsy Forceps
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Reprocessed Electric Biopsy Forceps
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
POWDER FREE TEXTURED VINYL EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
AESCULAP -MIETHKE SHUNT SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·LCS TOTAL KNEE SYSTEM
Appliance, Fixation, Spinal Interlaminal
FDA classification
FDA Class 2
·Appliance, Fixation, Spinal Interlaminal
Shunt, Central Nervous System And Components
FDA classification
FDA Class 2
·Shunt, Central Nervous System And Components
Vinyl Patient Examination Glove
FDA classification
FDA Class 1
·Vinyl Patient Examination Glove