Primary Device ID | G51017960 |
NIH Device Record Key | 213171fe-d389-4781-b1c9-93b0b99cc668 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UV POWER |
Version Model Number | 1796 |
Company DUNS | 075058495 |
Company Name | Light Sources, Inc. |
Device Count | 1 |
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 | 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 | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | G51017960 [Primary] |
LEJ | Booth, Sun Tan |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-20 |
Device Publish Date | 2024-12-12 |
G51024590 | 2459 |
G51024090 | 2409 |
G5102578 | FR2000T12/VHO/BP/8.5/230 200W |
G51017960 | 1796 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UV POWER 78504180 3221304 Dead/Cancelled |
UV-POWER LICHT GMBH 2004-10-22 |
UV POWER 76269502 not registered Dead/Abandoned |
UV POWER, L.C. 2001-06-11 |