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KWIK-STIK™ and LYFO DISK™

EUDAMEDFDA UDI

Class B (EU MDR)

Ref [0527U] KWIK-STIK™ C. difficile ATCC 700057™Model 0527

by Microbiologics, INC.

Identity

Trade Name
KWIK-STIK™ FDA UDI
Generic Name
Multiple bacteria species culture isolate identification control IVD, kit FDA UDI
Device Name
KWIK-STIK™ and LYFO DISK™ EUDAMED
KWIK-STIK™ C. difficile ATCC 700057™ FDA UDI
Model / Reference
0527 EUDAMED
[0527U] KWIK-STIK™ C. difficile ATCC 700057™ EUDAMED
0527U FDA UDI
Description
KWIK-STIK™ C. difficile ATCC 700057™ FDA UDI

Identifiers

Catalog Number
0527U FDA UDI
Primary DI / UDI-DI
10845357012781 EUDAMEDFDA UDI
Basic UDI-DI
0845357005279Z EUDAMED
FDA Product Code
JTR FDA UDI
EMDN Code
W01040601 QC STRAINS BACTERIOLOGY EUDAMED
GMDN Term
Multiple bacteria species culture isolate identification control IVD, kit FDA UDI

Classification

Device Class
Class B EUDAMED
Class I FDA UDI
Regulation Number
866.2480 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

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

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 06587b57-158c-4c1a-a455-444d25cc8d84 61 fields · synced Jun 19, 2026
  • FDA UDI 8cd5a5c9-f1aa-4193-89b0-b3d5c326b5bb 36 fields · synced May 30, 2026