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KWIK-STIK™ and LYFO DISK™

EUDAMEDFDA UDI

Class B (EU MDR)

Ref [0322U] KWIK-STIK™ P. anaerobius ATCC 27337™Model 0322

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™ P. anaerobius ATCC 27337™ FDA UDI
Model / Reference
0322 EUDAMED
[0322U] KWIK-STIK™ P. anaerobius ATCC 27337™ EUDAMED
0322U FDA UDI
Description
KWIK-STIK™ P. anaerobius ATCC 27337™ FDA UDI

Identifiers

Catalog Number
0322U FDA UDI
Primary DI / UDI-DI
10845357006353 EUDAMEDFDA UDI
Basic UDI-DI
0845357003229D 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 76eaa1d5-360f-4dde-b699-efad4e716e1d 61 fields · synced Jul 11, 2026
  • FDA UDI 85cb112e-fb89-439d-a4bd-3c9713dc8fed 36 fields · synced May 30, 2026