21 results
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47ms
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Sources: EU EUDAMED, US FDA
Collector, Urine, (and Accessories) for Indwell Cath/ Tray, Catheteriz, Sterile Urethral, w/wo Catheter (kit)- DeRoyal
FDA registration
DeRoyal Industries, Inc.·2 products·🇺🇸 United States
Collector, Urine, (and Accessories) for Indwell Cath/ Tray, Catheteriz, Sterile Urethral, w/wo Catheter (kit)- DeRoyal
FDA registration
DEROYAL INDUSTRIES, INC.·2 products·🇺🇸 United States
Collector, Urine, (and Accessories) for Indwell Cath/ Tray, Catheteriz, Sterile Urethral, w/wo Catheter (kit)- DeRoyal
FDA registration
DEROYAL INDUSTRIES, INC.·2 products·🇺🇸 United States
Collector, Urine, (and Accessories) for Indwell Cath/ Tray, Catheteriz, Sterile Urethral, w/wo Catheter (kit)- DeRoyal
FDA registration
DeRoyal Industries, Inc.·2 products·🇺🇸 United States
Collector, Urine, (and Accessories) for Indwell Cath/ Tray, Catheteriz, Sterile Urethral, w/wo Catheter (kit)- DeRoyal
FDA registration
DEROYAL INDUSTRIES, INC.·2 products·🇺🇸 United States
UROLOGICAL CATHETER & ACCESSORIES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)
FDA classification
FDA Class 2
·Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)
QP-101BK
FDA registration
Nihon Kohden Corporation - Eastern Japan Logistics Center·1 product·🇯🇵 Japan
HOWMEDICA OSTEONICS CORP
FDA registration
HN AND M GMBH·1 product·🇨🇭 Switzerland
QP-101BK
FDA registration
Nihon Kohden Corporation - Tokorozawa establishment Advanced Technology Center·1 product·🇯🇵 Japan
QP-101BK
FDA registration
NIHON KOHDEN AMERICA, INC.·1 product·🇺🇸 United States
QP-101BK
FDA registration
NIHON KOHDEN TOMIOKA PRODUCTION CENTER·1 product·🇯🇵 Japan
QP-101BK
FDA registration
Nihon Kohden America Fulfillment Center·1 product·🇺🇸 United States
QP-101BK
FDA registration
Nihon Kohden Tomioka Corporation·1 product·🇯🇵 Japan
STRYKER GmbH
FDA registration
STRYKER GmbH·1 product·🇨🇭 Switzerland
Synergy Health Daniken AG
FDA registration
Synergy Health Daniken AG·1 product·🇨🇭 Switzerland
QP-101BK
FDA registration
NIHON KOHDEN CORP.·1 product·🇯🇵 Japan
MEE-1000A NEUROMASTER
FDA 510(k)
FDA Class 2
·Neurology
VariAx 2 Wrist Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
Stimulator, Electrical, Evoked Response
FDA classification
FDA Class 2
·Stimulator, Electrical, Evoked Response