- Role
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EUDAMED last updated this device on Apr 21, 2026
805630062FTPR169FSIROP TOUX ENFANT BIOGARAN CONSEIL® 120 mL FR is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Labomar S.p.A.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08056300621874805630062FTPR169FFTPR16(01)08056300621874
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES1 warning recorded — scroll inside the panel to see all entries.
CW999Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market |
IT-MF-000007965Certificate health across this manufacturer's portfolio.
CSQ0026240724SupplementedCSQ0026240424