37 results
·
43ms
·
Sources: EU EUDAMED, US FDA
Silicone Rectal Balloon
FDA registration
Cook Incorporated·1 product·🇺🇸 United States
Silicone Rectal Balloon
FDA registration
Cook Incorporated·1 product·🇺🇸 United States
SILICONE RECTAL BALLOON
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Device, Cystometric, Hydraulic
FDA classification
FDA Class 2
·Device, Cystometric, Hydraulic
Invictus
FDA UDI
ALPHATEC SPINE, INC.·00190376309132·Cross Connector, Head to Head, 35mm
Cranial Fusion Plate System
FDA UDI
Life Spine, Inc.·00190837031381·35mm Plate
PLIF Allograft
FDA UDI
SEASPINE ORTHOPEDICS CORPORATION·10889981087661·13mm Trial
B. BRAUN MEDICAL INC.
FDA registration
B. BRAUN MEDICAL INC.·1 product·🇺🇸 United States
Sterigenics U.S., LLC
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
VYAA
FDA registration
VYGON USA·1 product·🇺🇸 United States
ISOMEDIX OPERATIONS INC.
FDA registration
ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States
VYAA
FDA registration
Vygon MFG·1 product·🇺🇸 United States
B. BRAUN US DEVICE MANUFACTURING LLC
FDA registration
B. BRAUN US DEVICE MANUFACTURING LLC·1 product·🇺🇸 United States
Informer Med Steam PCD (FP-CFE)
FDA registration
STERIS Corporation·1 product·🇺🇸 United States
Sterigenics U.S., LLC
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Informer Med Steam PCD (FP-CFE)
FDA registration
STERIS Corporation·1 product·🇺🇸 United States
B. BRAUN MEDICAL INC.
FDA registration
B. BRAUN MEDICAL INC.·1 product·🇺🇸 United States
Grasping forceps
FDA UDI
SOPRO-COMEG GmbH·04059082022963·
DANA REUSABLE BI TEST PACK
FDA 510(k)
FDA Class 2
·General Hospital
SAFETY INTRODUCER NEEDLE
FDA 510(k)
FDA Class 2
·Cardiovascular