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ST355JH Procedure set

by STS Medical Group EAD

Ref 29931Model SECUTRAY

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number380023TD03GENIIAXJ Basic UDI-DI 03800232425056UDI-DIDate23 Jun 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  • Withdrawn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
General surger, Sterile
Model / Reference
SECUTRAY, 29931
Primary DI / UDI-DI
03800232425056
Basic UDI-DI
380023TD03GENIIAXJ
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class IIa
Medical Purpose
Sterile, disposable procedure pack, combination of devices for injury or disease treatment related to general surgery.

Manufacturer details

EUDAMED SRN
BG-PR-000041814

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Properties

  • Sterile