- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 12, 2026
697530902DGKQGM1 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by NINGBO ANNMY MEDICAL PRODUCTS CO.,LTD. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
16975309029162697530902DGKQGM1(01)16975309029162
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.
U0899GYNAECOLOGICAL DEVICES - OTHERNo 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 | Feb 21, 2026 | Jun 12, 2026 |
CN-MF-000044387No 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.