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Image intensifier drape pack Siemens

by STS Medical Group EAD 2 variants

Ref D020001Model 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 linked in EUDAMED

A group certificate may exist

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 Number380023TD04TIPEST8R Basic UDI-DI 03800238373771UDI-DIDate27 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Table and instrument drapes, Sterile, Viscose nonwoven, PE coex film, virgin cellulose
Model / Reference
SECUDRAPE, D020001
Primary DI / UDI-DI
03800238373771
Basic UDI-DI
380023TD04TIPEST8R
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

  • 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