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Instrument table

by S.E.S Healthcare products (Lingbi) Co., Ltd

Ref P-40-0101-CHModel B002

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 Number697452367B002EN Basic UDI-DI 26974523670706UDI-DIDate22 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  • Withdrawn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

Device Name
Surgical Drape
Model / Reference
B002, P-40-0101-CH
Primary DI / UDI-DI
26974523670706
Basic UDI-DI
697452367B002EN
EMDN Code
T020199 Surgical drapes - other
Device Class
Class I
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CN-MF-000001143
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from S.E.S Healthcare products (Lingbi) Co., Ltd

See all devices from S.E.S Healthcare products (Lingbi) 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