Primary Device ID | G5103105 |
NIH Device Record Key | 1ba1b79c-2d10-4693-bdd3-8a542b361346 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MEGALINE |
Version Model Number | 3105 |
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 | G5103105 [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 | 2024-09-18 |
Device Publish Date | 2024-09-10 |
G51031220 | 3122 |
G5103105 | 3105 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEGALINE 77317197 not registered Dead/Abandoned |
SPIELO INTERNATIONAL CANADA ULC 2007-10-30 |
MEGALINE 74274906 not registered Dead/Abandoned |
KSB Aktiengesellschaft 1992-05-12 |