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HTI Lytic

EUDAMED

Class A (EU MDR)

Ref 11-81

by High Technology Inc.

Identity

Trade Name
HTI Lytic EUDAMED
Device Name
HTI Lytic Reagent EUDAMED
Model / Reference
11-81 EUDAMED

Identifiers

Primary DI / UDI-DI
00860008666338 EUDAMED
Basic UDI-DI
08600086663HERELYT1WP EUDAMED
Direct Marketing DI
00860008666338 EUDAMED
EMDN Code
W0202010185 AUTOMATED WHOLE BLOOD HEMATOLOGY ANALYSERS - CONSUMABLES EUDAMED

Classification

Device Class
Class A 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

New Device

No

EUDAMED

HTI Lytic by High Technology Inc. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
US-MF-000036184
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED b15535ae-ac8d-43f7-abe1-ea4abf7dacc2 61 fields · synced Jun 20, 2026