| Primary Device ID | 02816901023820 |
| NIH Device Record Key | c36f0838-b76e-4e37-a786-51240dabddc7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PSS Urology, Inc. |
| Version Model Number | WFS-365-RTSB |
| Catalog Number | 095897 |
| Company DUNS | 039281260 |
| Company Name | Weinert Fiber Optics, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816901023822 [Primary] |
| GS1 | 01816901023821 [Package] Contains: 00816901023822 Package: [5 Units] In Commercial Distribution |
| GS1 | 02816901023820 [Package] Contains: 01816901023821 Package: [2 Units] In Commercial Distribution |
| GEX | Powered laser surgical instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-05-02 |
| Device Publish Date | 2023-01-01 |
| 02816901023677 - Typenex Medical | 2025-04-01 |
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| 02816901024056 - NeuLight® | 2024-12-30 |
| 02816901023660 - Typenex Medical | 2024-11-11 |
| 01816901023975 - NeuLight® | 2024-05-20 |
| 02816901023967 - NeuLight® | 2024-05-13 |
| 01816901023395 - NeuLight® | 2024-02-12 |
| 01816901023722 - NeuLight® | 2023-10-03 |