10,000 results
·
458ms
·
Sources: EU EUDAMED, US FDA
Hercules
FDA UDI
MOREL COMPANY, LLC., THE·00819552020059·35" VersaCare Patient Repositioner
Baby Buddha
FDA UDI
BABYBUDDHA PRODUCTS LLC·00867494000417·Comfort Double Electric
Hercules
FDA UDI
MOREL COMPANY, LLC., THE·M988DVSA5·35" Width VersaCare Patient Repositioner
Hercules
FDA UDI
MOREL COMPANY, LLC., THE·M988DFSA9·39" Width Flat Patient Repositioner
Hercules
FDA UDI
MOREL COMPANY, LLC., THE·00819552020004·33" Width Flat Deck Patient Repositioner
Hercules
FDA UDI
MOREL COMPANY, LLC., THE·M988DFSA3N·33" Width Flat Patient Repositioner
Hercules
FDA UDI
MOREL COMPANY, LLC., THE·M988DFSA5·35" Width Flat Patient Repositioner
Hercules
FDA UDI
MOREL COMPANY, LLC., THE·M988DFSA3R·33" Width Raised Patient Repositioner
Dot Pad
Device
EU MDR
·
Eu Md Class 1
·Dot Incorporation·On the market
Faniel
FDA registration
FANIEL INC.·1 product·🇨🇦 Canada
Green Chem (Viet Nam) Co., LTD
FDA registration
Green Chem (Viet Nam) Co., LTD·1 product·🇻🇳 Vietnam
Faniel
FDA registration
FANIEL INC.·1 product·🇨🇦 Canada
BESTWAY
FDA registration
BESTWAY·1 product·🇭🇰 Hong Kong
AOT EXTERNAL COMPRESS DEVICE
FDA 510(k)
FDA Class 1
·Orthopedic
Kit, Identification, Neisseria Gonorrhoeae
FDA Pre-Market Approval
FDA Class 1
·GONOSTICON DRI-DOT
Status Mono
FDA registration
PRINCETON BIOMEDITECH CORP.·1 product·🇺🇸 United States
AccuSign MET
FDA registration
PRINCETON BIOMEDITECH CORP.·1 product·🇺🇸 United States
LifeSign Plus
FDA registration
PRINCETON BIOMEDITECH CORP.·1 product·🇺🇸 United States
Status First Strep A
FDA registration
PRINCETON BIOMEDITECH CORP.·1 product·🇺🇸 United States
StatusFirst CHF NT-proBNP
FDA registration
PRINCETON BIOMEDITECH CORP.·1 product·🇺🇸 United States