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Lind-Vac

by OÜ InterVacTechnology 554 variants

Ref AG2402

Lind-Vac (AG2402) is a device classified as IVD General made by OÜ InterVacTechnology, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-04744489012029), active as of 7 Nov 2026.

Active European Union

CE IVDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-04744489012029 Basic UDI-DI Date30 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDD Active

Specification

EUDAMED

Device name
Vacuum blood collection tube Lind-Vac® 13x100 mm clot activator & gel x 4 ml, yellow cap, sterile, two-part
Vacuum blood collection tube Lind-Vac® 13x100 mm clot activator & gel x 4 ml, red cap, sterile, two-part
Model / reference
AG2402
Primary DI / UDI-DI
04744489012029, 04744489015747
Basic UDI-DI
B-04744489012029, B-04744489015747
EMDN code
W050101010201 Blood collection, tubes with additives or serum separator
Device class
Class IVD General
EU registration type
Legacy device (under a directive)
EU market of registration
Estonia

Manufacturer details

EUDAMED SRN
EE-MF-000001021

Similar devices in this category

Other devices filed under BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR.

Other devices from OÜ InterVacTechnology

See all devices from OÜ InterVacTechnology →

Properties

  • Supplied sterile
  • Professional testing
Other properties (11, all answered No)