43 results
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54ms
·
Sources: EU EUDAMED, US FDA
REV-MED Inc.
Manufacturer
🇰🇷 South Korea·6 Basic UDI-DIs·6 Devices·Szutest Uygunluk Değerlendirme A.Ş. and TÜV SÜD Product Service GmbH
REV-MED INC.
FDA registration
REV-MED INC.·1 product·🇰🇷 South Korea
TriCell PRP
Device
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·On the market·1 country
TriCell PRP
Device
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·On the market·1 country
TriCell PRP
Device
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·On the market·1 country
THERAPEUTIC LASERS
Device
EU MDD
·
Eu Md Class 2b
·REV-MED Inc.·On the market·1 country
Tricell PRP
Device
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·On the market·1 country
Tricell PRP
Device
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·On the market·1 country
Hilthera 4.0
FDA UDI
REV-MED Inc.·08809326582113·
Blood Separation Kit
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·1 device
Blood Separation Kit
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·1 device
Blood Separation Kit
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·1 device
Therapeutical Laser Unit
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·REV-MED Inc.·1 device
Blood Separation Kit
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·1 device
Blood Separation Kit
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·REV-MED Inc.·1 device
2195-MED-2012004
Certificate
MDD Annex II (excluding section 4)·REV-MED Inc.·Szutest Uygunluk Değerlendirme A.Ş.·1 Basic UDI-DI
G1 095551 0002
Certificate
MDD Annex II (excluding section 4)·REV-MED Inc.·TÜV SÜD Product Service GmbH·5 Basic UDI-DIs
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·August 28, 2024
QDOT MICRO
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code OAE·August 28, 2024
TI LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code NKG·June 23, 2017