26 results
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41ms
·
Sources: EU EUDAMED, US FDA
Ion Endoluminal System (Ion Fully Articulating Catheter) (IF1000)
FDA registration
INTUITIVE SURGICAL, INC.·1 product·🇺🇸 United States
Ion Endoluminal System (Ion Fully Articulating Catheter) (IF1000)
FDA registration
Intuitive Surgical, S. De R.L. De C.V.·1 product·🇲🇽 Mexico
Ion Endoluminal System (Ion Fully Articulating Catheter) (IF1000)
FDA registration
Intuitive Surgical, S. de R.L. de C.V.·1 product·🇲🇽 Mexico
Ion Endoluminal System (Ion Fully Articulating Catheter) (IF1000)
FDA registration
INTUITIVE SURGICAL, INC.·1 product·🇺🇸 United States
Ion Endoluminal System (Ion Fully Articulating Catheter) (IF1000)
FDA registration
INTUITIVE SURGICAL, INC.·1 product·🇺🇸 United States
Ion Endoluminal System (Ion Fully Articulating Catheter) (IF1000)
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·00636257125809·30-40 MV FOR MEN CLSC CALF STD TAN V
Delta®
FDA UDI
MEDTRONIC PS MEDICAL, INC.·00613994908070·SHUNT 24013-5 DELTA UNITIZED RGL
Delta®
FDA UDI
MEDTRONIC PS MEDICAL, INC.·00643169472815·SHUNT 24013-5 DELTA UNITIZED RGL
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117391·Modular Knee Stem Pilot 13mm x 150mm
Systagenix Wound Management, Limited
FDA registration
Systagenix Wound Management, Limited·1 product·🇬🇧 United Kingdom
Tiga SUB4
FDA registration
SUNRISE MEDICAL (US) LLC·1 product·🇺🇸 United States
Systagenix Wound Management Manufacturing Limited
FDA registration
Systagenix Wound Management Manufacturing Limited·1 product·🇬🇧 United Kingdom
Tiga SUB4
FDA registration
Sunrise Medical (US) LLC·1 product·🇺🇸 United States
3M Deutschland GmbH
FDA registration
3M Deutschland GmbH·1 product·🇩🇪 Germany
SANICURE BV
FDA registration
SANICURE BV·1 product·🇳🇱 Netherlands
Tiga SUB4
FDA registration
RGK WHEELCHAIRS, LTD.·1 product·🇬🇧 United Kingdom
Bronchoscope (Flexible Or Rigid)
FDA classification
FDA Class 2
·Bronchoscope (Flexible Or Rigid)
AVANOS
FDA UDI
Avanos Medical, Inc.·00609038200866·BALLARD* Seal Cassette Replacement for Closed S...
SacroFuse
FDA UDI
SPINEFRONTIER, INC.·00190361023388·Ø10MM SLOTTED FUSION SCREW, GEN II, SACROFUSE, ...