6,900 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH(R)II MODELS 262-16
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH(R) II IMPLANT. PACEMAKER PULSE GENERATOR
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·CYBERTACH(TM) 60 PULSE GENERATOR & PROGRAMMER
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·TELECTRONICS PASAR MODEL 4171 PG
Sperm SP10 protein detection device
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Zhejiang Wantaifu Biotechnology Co., Ltd·1 device
Implant, Intragastric For Morbid Obesity
FDA Pre-Market Approval
FDA Class 3
·LAP-BAND ADJUSTABLE GASTRIC BANDING (LAGB) SYSTEM
ThermaChem HT2000
FDA registration
RELITECH B.V.·1 product·🇳🇱 Netherlands
TouchChat HD w/ WordPower App
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·PRENTKE ROMICH COMPANY·10 devices
ADULT-SINGLE-HHW-WITH CB
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Foxxmed Ltd·1 device
ADULT-DUAL-HHW-WITH CB
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·Foxxmed Ltd·1 device
Pocket Mask O2 HC w/o wipe (CDN)
FDA UDI
Laerdal Medical AS·07045430079694·The Pocket Mask is primarily designed for mouth...
AUTO REF/KERATO/TONOMETER
FDA UDI
NIDEK CO.,LTD.·04987669100066·AUTO REF/KERATO/TONOMETER Model TONOREF II is d...
VINYL PATIENT EXAMINATION GLOVE, POWDER-FREE
FDA 510(k)
FDA Class 1
·General Hospital
VINYL PATIENT EXAMINATION GLOVE, POWDERED
FDA 510(k)
FDA Class 1
·General Hospital
FibreKor Fiber Post Drill
FDA registration
Kerr Corporation·1 product·🇺🇸 United States
FibreKor Fiber Post Drill
FDA registration
Kerr Corporation·1 product·🇺🇸 United States
FibreKor Fiber Post Drill
FDA registration
Kerr Italia, S.r.l.·1 product·🇮🇹 Italy
FibreKor Fiber Post Drill
FDA registration
Ormex S. de R.L. de C.V.·1 product·🇲🇽 Mexico
Compumedics Somte System
FDA registration
COMPUMEDICS LIMITED·1 product·🇦🇺 Australia
Orion LifeSpan MEG
FDA registration
COMPUMEDICS LIMITED·1 product·🇦🇺 Australia