Primary Device ID | 00859626006091 |
NIH Device Record Key | 12673c65-cfea-4a81-b1a4-e42832842b51 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | ML-830-01-013 |
Catalog Number | ML-830-01-013 |
Company DUNS | 137829417 |
Company Name | MICROLIGHT CORPORATION OF AMERICA |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | 281-433-4648 |
XX@XX.XX |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00859626006091 [Primary] |
NHN | Powered Light Based Non-Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-08-15 |
00859626006015 - ML 830® | 2020-02-06 Charging Station |
00859626006299 - ML 830® | 2020-02-06 SL Power Supply |
00859626006121 - GlobTek | 2019-10-07 Transformer with Output Cord |
00859626006343 - ML 830® | 2019-04-22 Smart Laser DP |
00859626006336 - ML 830® | 2019-04-15 Laser Probe Cover |
00859626006008 - ML 830® | 2019-01-08 Battery Unit |
00859626006046 - ML 830® | 2019-01-08 Laser Probe |
00859626006107 - ML 830® | 2019-01-08 Original Direct Connect |