| Primary Device ID | 26945630132524 |
| NIH Device Record Key | 0a4fe0fe-c90f-48fc-a408-60935ece0a10 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STERiLANCE LDE4 Lancing Device |
| Version Model Number | 02-2201 |
| Company DUNS | 554434897 |
| Company Name | Sterilance Medical (Suzhou) Inc. |
| Device Count | 1 |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 16945630132527 [Primary] |
| GS1 | 26945630132524 [Package] Contains: 16945630132527 Package: [50 Units] In Commercial Distribution |
| GS1 | 36945630132521 [Package] Package: [10 Units] In Commercial Distribution |
| 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 | 2024-10-31 |
| Device Publish Date | 2024-10-23 |