- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 20, 2026
6975447866975447860002U9Model:BVS-Pro W is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Chengdu Mediate Technology Co., Ltd.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069754478600026975447866975447860002U9Model:BVS-Pro W (01)06975447860002
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.
Z12080304ULTRASONIC BLADDER VOLUME SCANNERSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jul 9, 2024 | Dec 31, 2028 |
| Germany | May 31, 2026 | Dec 31, 2028 |
CN-MF-000041946No 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.