- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 20, 2026
697122740SPNRKVerifine is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Promisemed Hangzhou Meditech Co., Ltd.. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06971227400789697122740SPNRKDPN-29*8(01)06971227400789
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.
A0101010201HYPODERMIC PEN NEEDLES, WITH SAFETY SYSTEMS3 warnings recorded — scroll inside the panel to see all entries.
CW030CW009CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Denmark; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | Nov 4, 2015 | Still on market |
| Finland | Nov 4, 2015 | Still on market |
| Italy | Still on market | |
| Sweden | Nov 4, 2015 | Still on market |
CN-MF-000008465No 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.