| Primary Device ID | 06945630108990 |
| NIH Device Record Key | 9deaa690-4dd2-494d-a8a6-70ae9144cf9e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sterilance Press4 Pressure Activated Safety Lancet |
| Version Model Number | 05-081720B |
| Company DUNS | 421141183 |
| Company Name | SteriLance Medical (Suzhou) Inc. |
| Device Count | 100 |
| 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 |