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T Cell Receptor Gamma Gene Rearrangement

EUDAMED

Class IVD General (EU MDR)

Ref 9-207-0111

by Invivoscribe, Inc.

Identity

Trade Name
T Cell Receptor Gamma Gene Rearrangement EUDAMED
Device Name
T Cell Receptor Gamma Gene Rearrangement Assay 2.0 Megakit EUDAMED
Model / Reference
9-207-0111 EUDAMED

Identifiers

Primary DI / UDI-DI
00850052003630 EUDAMED
Basic UDI-DI
B-00850052003630 EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria 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

T Cell Receptor Gamma Gene Rearrangement by Invivoscribe, Inc. — Class IVD General — 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

Manufacturer
Invivoscribe, Inc.
EUDAMED SRN
US-MF-000011736
Authorised Representative
IN VIVOSCRIBE TECHNOLOGIES FR-AR-000003774

Sources (1)

  • EUDAMED d60250f1-bcbc-45f6-af1b-4766aae89848 61 fields · synced Jun 17, 2026