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Ad-2310DA

by Alltion (Guangxi) Instrument Co., Ltd.

Part of a family of 14 devices: see the family page

Ref many

Ad-2310DA (many) is a medical device (EU MDR Class I; EMDN category colposcopes) made by Alltion (Guangxi) Instrument Co., Ltd., registered in EUDAMED on 20 Apr 2026 (Basic UDI-DI 697044351AC2000XW), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697044351AC2000XW Basic UDI-DI 06970443510289UDI-DIDate20 Apr 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Colposcope
Model / reference
many
Primary DI / UDI-DI
06970443510289
Basic UDI-DI
697044351AC2000XW
Direct marketing DI
06970443510289
EMDN code
Z12020703 Colposcopes
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000024670
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under COLPOSCOPES.

Other devices from Alltion (Guangxi) Instrument Co., Ltd.

See all devices from Alltion (Guangxi) Instrument Co., Ltd. →

Properties

Other properties (14, all answered No)