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SPOT-it TREC Screening Kit

by ImmunoIVD AB

Ref 12-2015-T

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-47350134361173 Basic UDI-DI 47350134361173UDI-DIDate14 Nov 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
12-2015-T
Primary DI / UDI-DI
47350134361173
Basic UDI-DI
B-47350134361173, 7350134361178Q
Direct Marketing DI
47350134361173
EMDN Code
W0106010199 Monogenetic disorders tests - other
Device Class
Class IVD General
Class C
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000034517

From the manufacturer

Manufacturer's product page: SPOT-itTM TREC & KREC Screening Kit Screening Solution for SCID, XLA

Other devices from ImmunoIVD AB

See all devices from ImmunoIVD AB →

Properties

  • Animal Tissues
  • Microbial Substances
  • Reagent
  • Professional Testing

Other properties (7)

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