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Catheterisation set

by STS Medical Group EAD 2 variants

Ref 22004Model 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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number380023TD06INJIMG Basic UDI-DI 03800232425285UDI-DIDate23 Jun 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  • Withdrawn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
Injection / Infusion, Non sterile
Model / Reference
SECUTRAY, 22004
Primary DI / UDI-DI
03800232425285
Basic UDI-DI
380023TD06INJIMG
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class I
Medical Purpose
Disposable procedure pack, combination of devices for disease alleviation related to injection and infusion.

Manufacturer details

EUDAMED SRN
BG-PR-000041814

Other devices from STS Medical Group EAD

See all devices from STS Medical Group EAD →

Properties

Other properties (1)

  • Sterile: No