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ŽLICA PS 2, 5; 3, 75 i 5ml, CE, TISAK PANDA

by TEHNOPRO d.o.o.

Ref 000214Model SPOON PS ,PANDA print

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 Number385888353SpoonPandaFrogTT Basic UDI-DI 03858883539554UDI-DIDate8 Mar 2023RegisteredStatusActive

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  • Withdrawn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
SPOON PS 2,5; 3,75 and 5ml, PANDA print
Model / Reference
SPOON PS, PANDA print, 000214
Primary DI / UDI-DI
03858883539554
Basic UDI-DI
385888353SpoonPandaFrogTT
EMDN Code
A99 Devices for administration, withdrawal and collection - other
Models / Variants
Device Class
Class I
EU market of registration
Croatia

Manufacturer details

EUDAMED SRN
HR-MF-000025711

Other devices from TEHNOPRO d.o.o.

Properties

  • Measuring Function

Other properties (12)

  • Sterile: No
  • 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
  • Incorporates Medicinal Product: No