32 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Country: France
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ANI Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
ANI Sensor V1 PLUS
Device
EU MDR
·
Eu Md Class 1
·MDoloris Medical Systems SAS·On the market
Protection de barrière à poser PositPro 90 cm anis
Device
EU MDR
·
Eu Md Class 1
·IDENTITES 49·On the market
Air Products SAS
Manufacturer
🇫🇷 France·1 Basic UDI-DI·1 Device·DNV Product Assurance AS
RespInnovation
Manufacturer
🇫🇷 France·1 Basic UDI-DI·1 Device·DNV Product Assurance AS
ANI-MR
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·MDoloris Medical Systems SAS·1 device
Masques à usage médical à élastiques Type II Verts Anis - Sachet de 10
Device
EU MDR
·
Eu Md Class 1
·VBI Sarl·On the market
Masques à usage médical à élastiques Type II Verts Anis - Boîte de 50
Device
EU MDR
·
Eu Md Class 1
·VBI Sarl·On the market
ANI Sensor V2
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·MDoloris Medical Systems SAS·1 device
ANI Sensor V1
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·MDoloris Medical Systems SAS·1 device
ANI Sensor V1 PLUS
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·MDoloris Medical Systems SAS·2 devices
GAMIDA TECH
Manufacturer
🇫🇷 France·4 Basic UDI-DIs·4 Devices·IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A.
DENTAL COMPONENTS EUROPE
Authorized representative
🇫🇷 France·1 Manufacturer·2 Devices
Ziwig
Importer
🇫🇷 France·1 Manufacturer
CEMO
Importer
🇫🇷 France·1 Manufacturer
RespIn 11
Device
EU MDD
·
Eu Md Class 2a
·RespInnovation·On the market·32 countries
Bulk liquid nitrogen
Device
EU MDD
·
Eu Md Class 2a
·Air Products SAS·On the market·2 countries
TDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862.2100). Intended use: Laboratory Information System (L.I.S)
FDA Enforcement
Class III
·Terminated·Technidata S.A.·July 24, 2013
NATECH
Importer
🇫🇷 France·11 Manufacturers
ROSA(TM) Robotized Stereotactic Assistant, Version 2.5 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial markers or optical registration. The system is intended for use by neurosurgeons to guide standard neurosurgical instruments. It is indicated for any neurosurgical condition in which the use of stereotactic surgery may be appropriate.
FDA Enforcement
Class II
·Terminated·MEDTECH SAS·June 13, 2018