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KWIK-STIK™ and LYFO DISK™

EUDAMEDFDA UDI

Class B (EU MDR)

Ref [0274U] KWIK-STIK™ S. paucimobilis ATCC 29837™Model 0274

by Microbiologics, INC.

Identity

Trade Name
KWIK-STIK™ and LYFO DISK™ EUDAMED
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™ S. paucimobilis ATCC 29837™ FDA UDI
Model / Reference
0274 EUDAMED
[0274U] KWIK-STIK™ S. paucimobilis ATCC 29837™ EUDAMED
0274U FDA UDI
Description
KWIK-STIK™ S. paucimobilis ATCC 29837™ FDA UDI

Identifiers

Catalog Number
0274U FDA UDI
Primary DI / UDI-DI
10845357005066 EUDAMEDFDA UDI
Basic UDI-DI
0845357002749T EUDAMED
FDA Product Code
JTR FDA UDI
EMDN Code
W0105080801 BACTERIOLOGY CONTROLS - INF.IMM. 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

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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 (2)

  • EUDAMED 4adb85ad-f3e0-421e-b186-3f6554f943e9 61 fields · synced Jul 15, 2026
  • FDA UDI 92ca1dd0-8e2c-486b-b231-8a4e1b18afca 36 fields · synced May 30, 2026