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Inlet Adapter

by Acare Technology Co., Ltd. 37 variants

Ref AC-PB-10Model AC-BS, AC-OA, AC-JP, AC-DN, AC-CH, AC-DS, AC-AF, AC-PB, AC-EV, AC-OQ, AC-CG, AC-BR

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471987274AC-xx-xxLG Basic UDI-DI 04719872749998UDI-DIDate28 May 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
AC-BS, AC-OA, AC-JP, AC-DN, AC-CH, AC-DS, AC-AF, AC-PB, AC-EV, AC-OQ, AC-CG, AC-BR, AC-PB-10
Primary DI / UDI-DI
04719872749998
Basic UDI-DI
471987274AC-xx-xxLG
EMDN Code
A070101 Suction tubing adapters and connectors
Device Class
Class I
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
TW-MF-000031298
Authorised representative
Surpass Biomedical Europe B.V. NL-AR-000038619

Other devices from Acare Technology Co., Ltd.

See all devices from Acare Technology Co., Ltd. →

Properties

  • Administering Medicine

Other properties (12)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No