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0.5 ml Micro Centrifuge Tube, Amber color, Sterile

by Accumax Lab Devices Private Limited

Ref ACT-005-B-S-A

Active European Union

CE IVDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-MCT4ME Basic UDI-DI D-MCT4MEUDI-DIDate28 May 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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Device Name
0.5 ml Micro Centrifuge Tube,Amber color, Sterile
Model / Reference
ACT-005-B-S-A
Primary DI / UDI-DI
D-MCT4ME
Basic UDI-DI
B-MCT4ME
EMDN Code
W02069002 Test tube apparatuses
Device Class
Class IVD General
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IN-MF-000028076
Authorised representative
mdi Europa GmbH DE-AR-000006218

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See all devices from Accumax Lab Devices Private Limited →

Properties

  • Sterile

Other properties (9)

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