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EUDAMED last updated this device on Apr 29, 2026
7332343200017DPRO®MERA WOUND & EYE WASH is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Aurena Laboratories AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
073323433004667332343200017D301420(01)07332343300466
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.
M04040101SALINE DRESSINGS, NON-COMBINED9 warnings recorded — scroll inside the panel to see all entries.
CW268CW157CW139CW999CW999CW999CW999CW999CW999No certificate specifically references this device's Basic UDI-DI.
Primary placement in Sweden; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Aug 13, 2024 | Jun 24, 2025 |
| Finland | Aug 13, 2024 | Jun 24, 2025 |
SE-MF-000002890No 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.