← Back to catalogue

KWIK-STIK™ and LYFO DISK™

EUDAMED

Class B (EU MDR)

Ref [01045P] KWIK-STIK™ S. diarizonae ATCC 29934™Model 01045

by Microbiologics, INC.

Identity

Device Name
KWIK-STIK™ and LYFO DISK™ EUDAMED
Model / Reference
01045 EUDAMED
[01045P] KWIK-STIK™ S. diarizonae ATCC 29934™ EUDAMED

Identifiers

Primary DI / UDI-DI
20845357032137 EUDAMED
Basic UDI-DI
0845357001045WE 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

Category: Multiple bacteria species culture isolate identification control IVD, kit

KWIK-STIK™ and LYFO DISK™ by Microbiologics, Inc. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Multiple bacteria species culture isolate identification control IVD, kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000000466
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (1)

  • EUDAMED 50755936-df31-4ac8-949c-6e4fe2e6ad01 61 fields · synced Jun 18, 2026