| Primary Device ID | 56949517070795 |
| NIH Device Record Key | 3ca5335e-2034-4b20-a2ae-27905ccee077 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | plusmed |
| Version Model Number | LF-TL-30 |
| Company DUNS | 421330121 |
| Company Name | Shandong Lianfa Medical Plastic Products CO.,LTD |
| Device Count | 10 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06949517006379 [Primary] |
| GS1 | 56949517070795 [Unit of Use] |
| FMK | Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature |
| 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 | 2023-07-24 |
| Device Publish Date | 2023-07-16 |
| 06949517009028 - One +Step | 2025-09-22 A convenience kit consisting of 1 One Step Lancing Device and 100 pcs 23g lancets |
| 56949517070894 - One +Step | 2025-07-07 |
| 56949517070900 - One +Step | 2025-07-07 |
| 56949517070917 - One +Step | 2025-07-07 |
| 06949517008878 - One +Step | 2025-07-07 |
| 56949517070887 - Twist Lancet(30G) | 2024-11-11 Sterile Lancet for Single Use (Box of 100 lancets), sterilized with Irradiation sterilization |
| 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 |