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Dr.ANA® disposable balloon inflation devices

by Anni and Anna Limited 3 variants

Ref AA-ID-A2530H-TB

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 Number489711186IDYD Basic UDI-DI 04897111860038UDI-DIDate10 Aug 2024RegisteredStatusActive

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  • Withdrawn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
Disposable balloon inflation devices
Model / Reference
AA-ID-A2530H-TB
Primary DI / UDI-DI
04897111860038
Basic UDI-DI
489711186IDYD
EMDN Code
C010401020180 Ptca balloon dilatation catheters - accessories
Device Class
Class I
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
HK-MF-000036709
Authorised representative
Ellecom GmbH DE-AR-000012869

Other devices from Anni and Anna Limited

See all devices from Anni and Anna Limited →

Properties

  • Sterile

Other properties (12)

  • 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