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EUDAMED last updated this device on May 12, 2026
697034167265HFelectrode pad is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by GMDASZ Manufacturing Co., Ltd.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06970341673574697034167265HFPSN2510D(01)06970341673574
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.
N010201TENS SYSTEM ELECTRODES1 warning recorded — scroll inside the panel to see all entries.
CW262No certificate specifically references this device's Basic UDI-DI.
Primary placement in Spain; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Still on market |
CN-MF-000011760No 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.