21 results · 44ms · Sources: EU EUDAMED, US FDA

Implantium

FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States

FX4810MLC

FDA registration
Dentium USA·1 product·🇺🇸 United States

FX4810MLC

FDA registration
DENTIUM CO., LTD.·1 product·🇰🇷 South Korea

DENTIUM CO., LTD. IMPLANTIUM

FDA 510(k)
FDA Class 2 ·Dental

Synergy Health AST, LLC

FDA registration
Synergy Health AST, LLC·1 product·🇺🇸 United States

MEDELA DOMINANT 35CI

FDA registration
MEDELA LLC·1 product·🇺🇸 United States

Synergy Health AST, LLC

FDA registration
Synergy Health AST, LLC·1 product·🇺🇸 United States

ALLOMATRIX

FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

ALLOMATRIX

FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

MEDELA DOMINANT 35CI

FDA registration
MEDELA AG·1 product·🇨🇭 Switzerland

MMT-511 PARADIGM Insulin Pump

FDA registration
MEDTRONIC MINIMED·1 product·🇺🇸 United States

Algidex IV Patch

FDA registration
Sterigenics US LLC·2 products·🇺🇸 United States

PROTECTOR 21, PROTECTOR 50, PROTECTOR 14, INJECTOR LUER LOCK, INFUSION ADAPTER

FDA 510(k)
FDA Class 2 ·General Hospital

DRY AC ACID CONCENTRATE MIX FOR BICARBONATE HEMODIALYSIS

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration
Sterigenics UK Limited·1 product·🇬🇧 United Kingdom

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States

ULTRAPERC PERCUTANEOUS SINGLE STAGE DILATION TRACHEOSTOMY PROCEDURE KIT WITH 7MM BLU TUBE +2/CA Portex UltraPerc Singl

FDA registration
Sterigenics Belgium Petit Rechain S.A.·1 product·🇧🇪 Belgium

Implant, Endosseous, Root-Form

FDA classification
FDA Class 2 ·Implant, Endosseous, Root-Form

Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

FDA classification
FDA Class 2 ·Dialysate Concentrate For Hemodialysis (Liquid Or Powder)