- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 28, 2026
695937380004NQCOM002 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by FITONE LATEX PRODUCTS CO., LTD. GUANGDONG. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06959373822334695937380004NQCOM002(01)06959373822334
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.
U110101CONDOMS1 warning recorded — scroll inside the panel to see all entries.
CW129No certificate specifically references this device's Basic UDI-DI.
This device is not currently linked to any other device.
Primary placement in Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | Jan 1, 2026 | Jan 1, 2030 |
CN-MF-000012805No 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.