Skip to content

Absorbent pad

by Shaoxing Yibon Medical Co., Ltd. 12 variants

Ref 2310008Model I

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6972370766900000S7 Basic UDI-DI 06937437814297UDI-DIDate19 Dec 2024RegisteredStatusActive

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  • Withdrawn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
I, 2310008
Primary DI / UDI-DI
06937437814297
Basic UDI-DI
6972370766900000S7
EMDN Code
M0202030102 Non-woven gauze pads, without x-ray detectable thread, non-sterile
Device Class
Class I
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
CN-MF-000003378
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Shaoxing Yibon Medical Co., Ltd.

See all devices from Shaoxing Yibon Medical Co., Ltd. →

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