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 |
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02816901024056 - NeuLight® | 2024-12-30 |
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01816901023975 - NeuLight® | 2024-05-20 |
02816901023967 - NeuLight® | 2024-05-13 |
01816901023395 - NeuLight® | 2024-02-12 |
01816901023722 - NeuLight® | 2023-10-03 |