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EUDAMED last updated this device on May 11, 2026
B-06925830103568Rule 6 of MDD Annex IX is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Zhejiang Geyi Medical Instrument Co.,Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06925830103568B-06925830103568Rule 6 of MDD Annex IX(01)06925830103568
European Medical Device Nomenclature — the EU product classification assigned to this device.
K01010101TROCAR STANDARD, SINGLE-USE4 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW001CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Dec 12, 2024 | Dec 31, 2028 |
CN-MF-000020887No 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.HD 2057271-1