Lancing Device LF-LD-A
by Shandong Lianfa Medical Plastic Products CO., LTD 4 variants
Lancing Device LF-LD-A is a Class II device made by Shandong Lianfa Medical Plastic Products CO., LTD, listed in FDA GUDID since 30 Apr 2019 (UDI-DI 06949517001893), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06949517001893 | Date30 Apr 2019 | StatusListed |
Official records
- AccessGUDID record 06949517001893
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Lancing Device
- Generic name
- Manual blood lancing device, reusable
- Model / reference
- LF-LD-A
- Primary DI / UDI-DI
- 06949517001893
- FDA product code
- FMK
- GMDN term
- Manual blood lancing device, reusable
- Device class
- Class II
- Regulation number
- 878.4850
- GUDID distribution status
- In Commercial Distribution
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