Primary Device ID | G51029120 |
NIH Device Record Key | 59efca88-4ac9-42ae-a785-2c6323f45452 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SIGNATURE SERIES |
Version Model Number | 2912 |
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 | G51029120 [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 | 2024-06-13 |
Device Publish Date | 2024-06-05 |
G51015540 | 1554 |
G51030550 | 3055 |
G51030490 | 3049 |
G51029100 | 2910 |
G51029120 | 2912 |
G51029130 | 2913 |
G51029080 | 2908 |