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neopiston

by Yangzhou Fartley Medical Instrument Technology Co., Ltd.

Part of a family of 181 devices: see the family page

Ref 222805

neopiston (222805) is a Class I device made by Yangzhou Fartley Medical Instrument Technology Co., Ltd, registered in EUDAMED on 24 Mar 2026 (Basic UDI-DI 69709008510147Y), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69709008510147Y Basic UDI-DI 06936603226810UDI-DIDate24 Mar 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Disposable Endoscopy Adapter Sets
Model / reference
222805
Primary DI / UDI-DI
06936603226810
Basic UDI-DI
69709008510147Y
Direct marketing DI
06936603226810
EMDN code
G0380 Digestive endoscopy devices - accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000009371
Authorised representative
Prolinx GmbH DE-AR-000005129

Similar devices in this category

Other devices filed under DIGESTIVE ENDOSCOPY DEVICES - ACCESSORIES.

Other devices from Yangzhou Fartley Medical Instrument Technology Co., Ltd

See all devices from Yangzhou Fartley Medical Instrument Technology Co., Ltd →

Properties

  • Supplied sterile
Other properties (13, all answered No)