1,560 results
·
37ms
·
Sources: EU EUDAMED, US FDA
SteadyTemp
Device
EU MDD
·
Eu Md Class 1
·SteadySense GmbH·On the market
Kombinationsanlage Avantgarde
Device
EU MDD
·
Eu Md Class 2a
·Unbescheiden GmbH·On the market·32 countries
Kombinationsanlage 0.20-2
Device
EU MDD
·
Eu Md Class 2a
·Unbescheiden GmbH·On the market·32 countries
Kombinationsanlage Avantgarde 0.30-1
Device
EU MDD
·
Eu Md Class 2a
·Unbescheiden GmbH·On the market·32 countries
Kombinationsanlage 0.20-1
Device
EU MDD
·
Eu Md Class 2a
·Unbescheiden GmbH·On the market·32 countries
Hydroelektrisches Vierzellenbad
Device
EU MDD
·
Eu Md Class 2a
·Unbescheiden GmbH·On the market·32 countries
ELECTROMYOGRAPHS
Device
EU MDD
·
Eu Md Class 2a
·DeMeTec GmbH·On the market·32 countries
SAVIR Alpha Synch mobile (SASm)
Device
EU MDD
·
Eu Md Class 2a
·SAVIR GmbH·On the market·1 country
DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER
Device
EU MDD
·
Eu Md Class 2a
·JOANNEUM RESEARCH Forschungsgesellschaft mbH·On the market·3 countries
DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER
Device
EU MDD
·
Eu Md Class 2a
·JOANNEUM RESEARCH Forschungsgesellschaft mbH·On the market·3 countries
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
V. Mueller
FDA UDI
CAREFUSION 2200, INC·10885403188626·V. Mueller RECTAL UNIVERSAL RING RETRACTOR KIT ...
ASSI
FDA UDI
ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATION·00841645141099·Nerve and Tendon Set Fcps. Includes, 6 Nerve & ...
POSEIDON
FDA registration
Kreatech biotechnology b.v.·1 product·🇳🇱 Netherlands
40V033V495
FDA registration
Kreatech biotechnology b.v.·1 product·🇳🇱 Netherlands