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Control Kit - PHOS L1

EUDAMED

Class IVD General (EU MDR)

Ref 92-201353-00

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
Control Kit - PHOS L1 EUDAMED
Device Name
Control Kit - PHOS L1 EUDAMED
Model / Reference
92-201353-00 EUDAMED

Identifiers

Primary DI / UDI-DI
00850011135433 EUDAMED
Basic UDI-DI
B-00850011135433 EUDAMED
EMDN Code
W0101050299 SPECIFIC CONTROLS (CC) - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Control Kit - PHOS L1 by LGC Clinical Diagnostics, 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

EUDAMED SRN
US-MF-000029697
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (1)

  • EUDAMED 257f8fb8-92d7-4c55-afab-667317303da4 61 fields · synced Jun 19, 2026