Lgm International Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000045320 FEI 3004421347
- Devices
- 2
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Liqui-PREP® Collection Vials - 200 Ref 60-010
Regimes: CE IVDR Registry: EUDAMEDLiqui-PREP® Cytology Processing Kit - 300 Ref 30-300
Regimes: CE IVDR Registry: EUDAMED
Company details
- EUDAMED SRN
- US-MF-000045320
- FDA FEI number
- 3004421347
- EUDAMED status
- Active
- EUDAMED registered name
- LGM INTERNATIONAL, INC.
- EUDAMED abbreviated name
- LGM
- Registered address
- 295-A, North Drive, 32934, Melbourne, United States
- Website
- www.liquiprepreagents.com
- [email protected]
- Phone
- 3212540480
- PRRC contact
- Charles Langley
Frequently asked questions
How many devices does LGM INTERNATIONAL INC. have in the registry?
The registry currently lists 2 devices for LGM INTERNATIONAL INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list LGM INTERNATIONAL INC.'s devices?
Among its 2 most recently registered devices, LGM INTERNATIONAL INC. has devices listed in EUDAMED (2 devices).
What risk classes do LGM INTERNATIONAL INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for LGM INTERNATIONAL INC.'s devices are IVDR Class A. Each device page shows its own class and authorisation.
What are the newest devices from LGM INTERNATIONAL INC. in the registry?
The most recently registered devices listed for LGM INTERNATIONAL INC. include Liqui-PREP® Collection Vials - 200 and Liqui-PREP® Cytology Processing Kit - 300.