← Back to catalogue
KWIK-STIK™ and LYFO DISK™
EUDAMEDClass B (EU MDR)
Ref [01005K] KWIK-STIK™ K. pneumoniae ATCC BAA-1705™Model 01005
Identity
- Device Name
- KWIK-STIK™ and LYFO DISK™ EUDAMED
- Model / Reference
- 01005 EUDAMED[01005K] KWIK-STIK™ K. pneumoniae ATCC BAA-1705™ EUDAMED
Identifiers
- Primary DI / UDI-DI
- 30845357024580 EUDAMED
- Basic UDI-DI
- 0845357001005W2 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 | 0845357001005W2 | 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 459c8034-ace3-4b7c-ae68-cf1a847d7eef 61 fields · synced Jun 18, 2026