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Biopsy Adapter

by Canon Inc. 4 variants

Ref UAGV-030AModel UAGL-001AHA, UAGV020A, UAGV-023A, etc.

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4987670A0403RK Basic UDI-DI 04987670100970UDI-DIDate16 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Biopsy Adapter
Model / Reference
UAGL-001AHA, UAGV020A, UAGV-023A, etc., UAGV-030A
Primary DI / UDI-DI
04987670100970
Basic UDI-DI
4987670A0403RK
Direct Marketing DI
04987670100970
EMDN Code
A01020102 Aspiration fine needles and kits
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
JP-MF-000013254
Authorised representative
Canon Medical Systems Europe B.V. NL-AR-000010531

Other devices from Canon Inc.

See all devices from Canon Inc. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No