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