6,596 results · 44ms · Sources: EU EUDAMED, US FDA

RFT

FDA UDI
Shenzhen RF Tech Co., Ltd.·06938146600089·8ch Flex 40 Array

RFT

FDA UDI
Shenzhen RF Tech Co., Ltd.·06938146600027·1.5T 8ch Foot Ankle Coil

RFT

FDA UDI
Shenzhen RF Tech Co., Ltd.·06938146600072·8ch Flex 50 Array

RFT

FDA UDI
Shenzhen RF Tech Co., Ltd.·06938146600041·1.5T 8ch Flex 50 Array (A-port)

RFT

FDA UDI
Shenzhen RF Tech Co., Ltd.·06938146600140·The Knee Coil manufactured by Shenzhen RF Tech ...

RFT

FDA UDI
Shenzhen RF Tech Co., Ltd.·06938146600119·The 1.5T 24E Posterior Array by Shenzhen RF Tec...

QUADESSY

FDA registration
CLASSYS INC·3 products·🇰🇷 South Korea

EndyMed Pro Max include Shaper MAX, Mini-shaper MAX, FSR MAX, Intensif MAX, iFine MAX, Small MAX and Contour MAX

FDA registration
ENDYMED MEDICAL INC.·3 products·🇺🇸 United States

Hysolate

FDA UDI
Dent4You AG·07630392901154·Winged Standard Kit Latex w/o Instruments

Handling belt - medium

Basic UDI-DI
EU MDD · Eu Md Class 1 ·NRS Healthcare·1 device

Profiling Bed

Basic UDI-DI
EU MDD · Eu Md Class 1 ·NRS Healthcare·1 device

PATIENT EXAMINATION GLOVE

FDA 510(k)
FDA Class 1 ·General Hospital

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·COGNIS CRT-D, LIVIAN CRT-D, CONTAK RENEWAL 3 RF HE CRT-D

BRF for cobas 8100

Basic UDI-DI
EU IVDR · Eu Ivd Class A ·Hitachi High-Tech Corporation·1 device

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK RENEWAL, CONTAK RENEWAL 3, CONTAK RENEWAL 3 RF CARDIAC RESYNCHRONIZATION THERAPY DEFIBRILLATOR SYSTEMS

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK RENEWAL/3/3 HE/3 RF/LIVIAN RF1 SE/CONTAK RENEWAL 3 AVT/COGNIS

Rheumatoid Factors 2 (RF 2)

Basic UDI-DI
EU IVDR · Eu Ivd Class B ·Thermo Fisher Scientific Oy·1 device

Chariot brancard TROLLER 2RP+2RF

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Contact Sécurité·7 devices

Rheumatoid Factors 2 (RF 2)

Basic UDI-DI
EU IVDD · Eu Ivd General ·Thermo Fisher Scientific Oy·1 device

Fraxis Duo ARM

FDA UDI
ILOODA.CO.,LTD·08800023200027·FRX 2.0 Articualed Arm