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HLAssure SE DPB1 Locus SBT Kit

EUDAMED

Class IVD Annex II List B (EU MDR)

Ref 50610

by TBG Biotechnology Corp.

Identity

Trade Name
HLAssure SE DPB1 Locus SBT Kit EUDAMED
Device Name
HLAssure SE DPB1 Locus SBT Kit EUDAMED
Model / Reference
50610 EUDAMED

Identifiers

Primary DI / UDI-DI
04718050361403 EUDAMED
Basic UDI-DI
B-04718050361403 EUDAMED
EMDN Code
W0106010401 HLA-TYPING EUDAMED

Classification

Device Class
Class IVD Annex II List B EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

HLAssure SE DPB1 Locus SBT Kit by TBG Biotechnology Corp. — Class IVD Annex II List B — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
TW-MF-000029664
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED 94c1e16d-47eb-4a99-9c5d-9c1b4eb7a8b1 61 fields · synced Jul 19, 2026