10,000 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Medline E-Z Lubricating Jelly Foil Pack 2.7G
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
SHANGHAI JPY ION-TECH CO., LTD.
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·2 products·🇨🇳 China
GLOBAL UNITE Platform Shoulder System
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·3 products·🇨🇳 China
Attune Dome Patella, ATTUNE MEDIAL DOME PAT 32MM
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
DEPUY SIGMA TIBIAL INSERTS AND CO-CR TIBIAL TRAYS
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
APEX HOLE ELIMINATOR PS
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
Duraloc
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
Allevyn Tracheostomy
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
SHANGHAI JPY ION-TECH CO., LTD.
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
SHANGHAI JPY ION-TECH CO., LTD.
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·1 product·🇨🇳 China
25MM VERSA-DIAL TAPER ADAPTOR
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·2 products·🇨🇳 China
CSTEM AMT
FDA registration
SHANGHAI JPY ION-TECH CO., LTD.·2 products·🇨🇳 China
Lens, Contact, Orthokeratology, Overnight
FDA Pre-Market Approval
FDA Class 3
·EUCLID SYSTEMS ORTHOKERATOLOGY (OPRIFOCON A) CONTACT LENSES FOR OVERNIGHT WEAR
Pulmeq sp. z o.o.
Manufacturer
🇵🇱 Poland·11 Basic UDI-DIs·13 Devices·TUV NORD Polska Sp. z o.o, TUV NORD Polska Sp. z o.o, and TUV NORD Polska Sp. z o.o
SILVERETTE MINI COPP ARG 2PZ
Device
EU MDR
·
Eu Md Class 1
·tecnologia ospedaliera srl·On the market·1 country
SILVERETTE MINI COPP ARG 2PZ
Device
EU MDR
·
Eu Md Class 1
·tecnologia ospedaliera srl·On the market
Water for Injection, EP/USP Sterile Grade
FDA UDI
INTERMOUNTAIN LIFE SCIENCES, LLC·B891WFIEPZ20L0·
Water for Injection, EP/USP Sterile Grade
FDA UDI
INTERMOUNTAIN LIFE SCIENCES, LLC·B891WFIEPZ2XL0·
ELECTRO-CAP W/CPZ EX SMALL
FDA UDI
ELECTRO-CAP INTERNATIONAL INC·00811478010121·
IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9
FDA 510(k)
FDA Class 2
·General, Plastic Surgery