- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 8, 2026
8712175_TD_11_SPSUPFS8578 / 8708 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Bevaplast B.V.. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
087121759413008712175_TD_11_SPSUPFS8578 / 8708(01)08712175941300
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.
M030499ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER2 warnings recorded — scroll inside the panel to see all entries.
CW010CW011No certificate specifically references this device's Basic UDI-DI.
Primary placement in Austria; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | May 8, 2026 | Still on market |
| Czechia | May 8, 2026 | Still on market |
| Germany | May 8, 2026 | Still on market |
| Netherlands | May 8, 2026 | Still on market |
NL-MF-000004386Certificate health across this manufacturer's portfolio.
2265082CE01Issued