12 results
·
45ms
·
Sources: EU EUDAMED, US FDA
PROBE 407 (307)
FDA registration
PERIMED AB·1 product·🇸🇪 Sweden
PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT
FDA 510(k)
FDA Class 2
·Cardiovascular
Flowmeter, Blood, Cardiovascular
FDA classification
FDA Class 2
·Flowmeter, Blood, Cardiovascular
Series 7000 Knee System
FDA registration
HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States
Tetric Ceram
FDA registration
Ivoclar Vivadent GmbH·1 product·🇩🇪 Germany
Tetric Ceram
FDA registration
IVOCLAR VIVADENT, INC.·1 product·🇨🇦 Canada
Tetric Ceram
FDA registration
IVOCLAR VIVADENT AG·1 product·🇱🇮 Liechtenstein
Alcon Contact Lens Case
FDA registration
AMCOR RIGID Packaging USA, LLC·1 product·🇺🇸 United States
CATHETER INTRODUCER MODIFICATION
FDA 510(k)
FDA Class 2
·Cardiovascular
MODEL 3500 MR-COMPATIBLE PULSE OXIMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Oximeter
FDA classification
FDA Class 2
·Oximeter
Introducer, Catheter
FDA classification
FDA Class 2
·Introducer, Catheter