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Image intensifier drape pack Siemens

by STS Medical Group EAD 2 variants

Ref D020001NSModel SECUDRAPE

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number380023TD04TIPENS88 Basic UDI-DI 03800238373689UDI-DIDate27 Jul 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  • Withdrawn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
Table and instrument drapes, Non-sterile, Viscose nonwoven, PE coex film, virgin cellulose
Model / Reference
SECUDRAPE, D020001NS
Primary DI / UDI-DI
03800238373689
Basic UDI-DI
380023TD04TIPENS88
EMDN Code
T030199 Covers, instruments and equipment - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
BG-MF-000041809

Other devices from STS Medical Group EAD

See all devices from STS Medical Group EAD →

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