Primary Device ID | 00806248007562 |
NIH Device Record Key | 127252ad-fd11-4c02-aed6-1c01cf508451 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Me |
Version Model Number | Series 15 |
Catalog Number | HU-FG01881 |
Company DUNS | 248047115 |
Company Name | Tanda Beauty Canada, Inc |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00806248006770 [Direct Marking] |
GS1 | 00806248007562 [Primary] |
GS1 | 10806248007569 [Package] Package: Inner Carton [3 Units] In Commercial Distribution |
GS1 | 20806248007566 [Package] Contains: 10806248007569 Package: Master Carton [4 Units] In Commercial Distribution |
OHS | Light Based Over The Counter Wrinkle Reduction |
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 | 2017-08-23 |
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