← Back to catalogue
KWIK-STIK™ and LYFO DISK™
EUDAMEDClass B (EU MDR)
Ref [0720K] KWIK-STIK™ V. furnissii NCTC 11218Model 0720
Identity
- Device Name
- KWIK-STIK™ and LYFO DISK™ EUDAMED
- Model / Reference
- 0720 EUDAMED[0720K] KWIK-STIK™ V. furnissii NCTC 11218 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 30845357017438 EUDAMED
- Basic UDI-DI
- 0845357007209V 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 0845357007209V | Class B | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Microbiologics, INC.
- EUDAMED SRN
- US-MF-000000466
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (1)
- EUDAMED e650ff0c-2d4b-4aaf-9677-b7dfc7fe9e3e 61 fields · synced Jun 18, 2026