| Primary Device ID | 56949517070108 |
| NIH Device Record Key | ea89441a-4d6d-4799-b523-a7942f79c209 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Safety lancet PAII(23G) |
| Version Model Number | LF-PAII-23 |
| Company DUNS | 421330121 |
| Company Name | Shandong Lianfa Medical Plastic Products CO.,LTD |
| Device Count | 25 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | 06949517003767 [Primary] |
| GS1 | 56949517070108 [Unit of Use] |
| FMK | Lancet, Blood |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2021-07-21 |
| Device Publish Date | 2020-04-21 |
| 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 |