Primary Device ID | G5101390 |
NIH Device Record Key | bbf4233a-2610-463c-b4be-7844b6f9d303 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SIGNATURE SERIES |
Version Model Number | 1390 |
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 | G5101390 [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 | 2024-10-14 |
Device Publish Date | 2024-10-04 |
G51015540 | 1554 |
G51030550 | 3055 |
G51030490 | 3049 |
G51029100 | 2910 |
G51029120 | 2912 |
G51029130 | 2913 |
G51029080 | 2908 |
G5101390 | 1390 |
G5101568 | FR2000/VHO/BP/2.4/210 |