10,000 results
·
103ms
·
Sources: EU EUDAMED, US FDA
Refraktionseinheit E-30 SE
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market·2 countries
Refraction unit E-30 SE
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market·2 countries
Refraktionseinheit E-30 SE
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market·2 countries
Refractionseinheit E-30 SE
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market·2 countries
Refraktionseinheit E-60
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market
Refraktionseinheit E-60
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market
Refraktionseinheit E-30 SE
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market·2 countries
Refraktionseinheit E-20 SE
Device
EU MDR
·
Eu Md Class 1
·bon Optic Vertriebsgesellschaft mbH·On the market
SONOTT FLOWLAB(R)
FDA 510(k)
FDA Class 2
·Cardiovascular
SONO TT ULTRASONIC FLOWCOMPUTER
FDA 510(k)
FDA Class 2
·Cardiovascular
ATOZ Mini-Screw(MKS-1608, MKS-1609, MKS-1610, MKS-1611, MKS-1612, MKS-1613, MKS-1614, MKS-1615, MKS-1616)
FDA registration
MK MEDITECH·1 product·🇰🇷 South Korea
ATOZ Key(MK Key-L, MK Key-S, MK Key-T-L, MK Key-T-S)
FDA registration
MK MEDITECH·1 product·🇰🇷 South Korea
ATOZ Drill bits(MKDB-F-08, MKDB-DG-08)
FDA registration
MK MEDITECH·1 product·🇰🇷 South Korea
ATOZ Expander(MKE-08-F, A-UNI-F08, T-UNI-F12)
FDA registration
MK MEDITECH·1 product·🇰🇷 South Korea
ATOZ Utility-wire(MK wire arm-1240, MK wire arm-1250, MK wire arm-1260)
FDA registration
MK MEDITECH·1 product·🇰🇷 South Korea
Mini Master Series
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746120282·DB BKT MINI MAND ANTERIOR 022 T-6 A=0 R=0 ON RA...
Mini Master Series
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746120275·DB BKT MINI MAND ANTERIOR 018 T-6 A=0 R=0 ON RA...
TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER
FDA 510(k)
FDA Class 2
·Ophthalmic
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·LATTITUDE PATIENT MANAGEMENT SYSTEM
face mask (except n95 respirator) for general public/healthcare personnel per iie guidance
FDA registration
A&A PRODUCT MANUFACTURING LIMITED·1 product·🇭🇰 Hong Kong