Primary Device ID | 05206569876055 |
NIH Device Record Key | 7a92585e-a698-4750-ab6c-f55f1b49d12a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BRIGHT LIGHT FLOW |
Version Model Number | A3.5, 2g |
Company DUNS | 728534814 |
Company Name | DMP DENTAL INDUSTRY S.A. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +302299023041 |
info@dmpdental.com |
Storage Environment Temperature | Between 4 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05206569000733 [Primary] |
GS1 | 05206569876055 [Package] Contains: 05206569000733 Package: Box [2 Units] In Commercial Distribution |
EBC | Sealant, Pit And Fissure, And Conditioner |
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 | 2016-09-24 |
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