| Primary Device ID | 06949517007024 |
| NIH Device Record Key | 7ae916a3-3984-466d-ac2f-e50bb7a4601d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N/M |
| Version Model Number | LDF |
| Company DUNS | 421330121 |
| Company Name | Shandong Lianfa Medical Plastic Products CO.,LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06949517007024 [Primary] |
| QRL | Multiple Use Blood Lancet For Single Patient Use Only |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-05 |
| Device Publish Date | 2024-05-28 |
| 06949517007024 - N/M | 2024-06-05Lancing Device(Bag of 1 devices) |
| 06949517007024 - N/M | 2024-06-05 Lancing Device(Bag of 1 devices) |
| 56949517070757 - Twist Lancet (30G) | 2024-04-01 Sterile Lancet for Single Use(Bag 10 lancets), Sterilized with Irradiation |
| 56949517070764 - Twist Lancet (30G) | 2024-04-01 Sterile Lancet for Single Use(Bag 50 lancets), Sterilized with Irradiation |
| 56949517070870 - Linkfar | 2024-03-27 |
| 06949517006362 - TysonBio | 2023-07-24 |
| 56949517070795 - plusmed | 2023-07-24 |
| 56949517070801 - TysonBio | 2023-07-24 |
| 56949517070818 - TysonBio | 2023-07-24 |