Skip to content

Probówka na 2, 5ml krwi, z heparyną Li, z nalepką, pakowane po 100 szt.

by MEDLAB-PRODUCTS Sp. z o.o.

Ref IP-32-0402-7N-100

Active European Union

CE IVDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5905072235070Z6 Basic UDI-DI 05905699563544UDI-DIDate29 May 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
Probówki do badań biochemicznych krwi w osoczu
Model / Reference
IP-32-0402-7N-100
Primary DI / UDI-DI
05905699563544
Basic UDI-DI
5905072235070Z6
EMDN Code
W050301020101 Samples analyses, plastic tubes with additives
Device Class
Class A
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000028388

Other devices from MEDLAB-PRODUCTS Sp. z o.o.

See all devices from MEDLAB-PRODUCTS Sp. z o.o. →

Properties

  • Professional Testing

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No