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Compresse piegate in tessuto non tessuto, confezionate in busta singola, 10 cm x 20 cm, 4 strati

by STS Medical Group EAD

Ref 20506Model SECUSORB

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number380023TD01TS0201TL Basic UDI-DI 03800232426701UDI-DIDate7 Oct 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  • Withdrawn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
Non-woven compresses non-invasive
Model / Reference
SECUSORB, 20506
Primary DI / UDI-DI
03800232426701
Basic UDI-DI
380023TD01TS0201TL
EMDN Code
M0202010101 Non-woven folded gauzes, without x-ray detectable thread, sterile
Device Class
Class IIa
EU market of registration
Italy

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