| Primary Device ID | 36945630136673 |
| NIH Device Record Key | f545370a-1d17-4e16-9f98-09ecdc9970fe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | suttersync |
| Version Model Number | soft 30G |
| Company DUNS | 554434897 |
| Company Name | Sterilance Medical (Suzhou) Inc. |
| Device Count | 50 |
| 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 | true |
| 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 | 06945630136672 [Unit of Use] |
| GS1 | 16945630136679 [Primary] |
| GS1 | 36945630136673 [Package] Contains: 16945630136679 Package: [200 Units] In Commercial Distribution |
| QRK | Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-02 |
| Device Publish Date | 2025-05-23 |
| 36945630137588 - index Asurity | 2025-09-03 |
| 36945630137595 - index Asurity | 2025-09-03 |
| 36945630137601 - index Asurity | 2025-09-03 |
| 36945630137618 - index Asurity | 2025-09-03 |
| 36945630139063 - index Asurity | 2025-09-03 |
| 36945630139070 - index Asurity | 2025-09-03 |
| 36945630137625 - index Asurity | 2025-09-02 |
| 36945630137632 - index Asurity | 2025-09-02 |