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Gripper kit

by STS Medical Group EAD

Ref 20030Model 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 Number380023TD06INJIIB4B Basic UDI-DI 03800232427517UDI-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  • Withdrawn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
Injection / Infusion, Non sterile
Model / Reference
SECUTRAY, 20030
Primary DI / UDI-DI
03800232427517
Basic UDI-DI
380023TD06INJIIB4B
EMDN Code
V0502 Clinical administration kits not included in other classes
Device Class
Class IIb
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