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EUDAMED last updated this device on May 26, 2026
8437015992UI0086GProfilm Aphtes AD (10mL) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by i+Med S.Coop.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
084366309901148437015992UI0086G-(01)08436630990114
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.
M04040501HYDROGEL DRESSINGS, NON-COMBINED7 warnings recorded — scroll inside the panel to see all entries.
CW010CW007CW032CW275CW277CW276CW999No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market |
ES-MF-000008633Certificate health across this manufacturer's portfolio.
2024 CR 0029Issued