Lyfo Disk™ 0736l
Ref [0736L] LYFO DISK™ S. cerevisiae NCYC 79Model 0736
Lyfo Disk™ 0736l is a device classified as Class B in the EU and Class I in the US made by Microbiologics, Inc., listed in FDA GUDID since 30 Apr 2020 (UDI-DI 10845357017595), registry data as of 23 Oct 2026.
Listed
CE, no status data
Valid until
Not applicable
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number10845357017595 | Date30 Apr 2020 | StatusListed |
Official records
- EUDAMED public site 10845357017595
- AccessGUDID record 10845357017595
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Lyfo Disk™
- Generic name
- Multiple bacteria species culture isolate identification control IVD, kit
- Device name
- KWIK-STIK™ and LYFO DISK™
- Model / Ref / Catalog
- 0736 EUDAMED[0736L] LYFO DISK™ S. cerevisiae NCYC 79 EUDAMED0736L GUDID
- Primary DI / UDI-DI
- 10845357017595
- Basic UDI-DI
- 084535700736AC
- FDA product code
- JTR
- EMDN code
- W01040699 Controls, standards, calibrators, microbiology - other
- GMDN term
- Multiple bacteria species culture isolate identification control IVD, kit
- Device class
- Class B EUDAMEDClass I GUDID
- Regulation number
- 866.2480
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 0736 [0736L] LYFO DISK™ S. cerevisiae NCYC 79 | 0736L |
| Device class | Class B | Class I |
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