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- Date of registration
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EUDAMED last updated this device on May 26, 2026
303144BAN875NDEC7BANDE COHESIVE is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by La Brosse et Dupont. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03031443126153303144BAN875NDEC7312615(01)03031443126153
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.
M0304010203ELASTIC COMPRESSION BANDAGES, COHESIVE, HIGH EXTENSIBILITY (>140%)3 warnings recorded — scroll inside the panel to see all entries.
CW009CW011CW083No 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 |
FR-MF-000004610No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.