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KWIK-STIK™ and LYFO DISK™

EUDAMED

Class B (EU MDR)

Ref [0629K] KWIK-STIK™ S. gallinarum ATCC 49148™Model 0629

by Microbiologics, INC.

Identity

Device Name
KWIK-STIK™ and LYFO DISK™ EUDAMED
Model / Reference
0629 EUDAMED
[0629K] KWIK-STIK™ S. gallinarum ATCC 49148™ EUDAMED

Identifiers

Primary DI / UDI-DI
30845357014871 EUDAMED
Basic UDI-DI
084535700629AA EUDAMED
EMDN Code
W01040601 QC STRAINS BACTERIOLOGY EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

New Device

No

EUDAMED

KWIK-STIK™ and LYFO DISK™ by Microbiologics, Inc. — Class B — 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-000000466
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (1)

  • EUDAMED 25a3c5fe-547c-4b35-8e7d-3a0069e22397 61 fields · synced Jun 19, 2026