Primary Device ID | G5102842 |
NIH Device Record Key | 1fcda27b-7024-46f1-a35d-55f001b2c210 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COSMETTA |
Version Model Number | 2842 |
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 | G5102842 [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 | 2024-12-27 |
Device Publish Date | 2024-12-19 |
G51028430 | 2843 |
G51028440 | 2844 |
G5102842 | 2842 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
COSMETTA 73563553 1404801 Dead/Cancelled |
VOLTARC TUBES, INC. 1985-10-16 |