Primary Device ID | 10074590542971 |
NIH Device Record Key | 2ab3010f-459f-43bb-9b23-edb11863436c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Remington Products |
Version Model Number | IPL6000Q-R |
Company DUNS | 001951946 |
Company Name | SPECTRUM BRANDS, 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 | false |
Serial Number | true |
Manufacturing Date | true |
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 | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx | |
Phone | 1-800-736-4648 |
xx@xx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00074590542974 [Primary] |
GS1 | 10074590542971 [Package] Contains: 00074590542974 Package: box [2 Units] In Commercial Distribution |
ONF | Powered Light Based Non-Laser Surgical Instrument With Thermal Effect |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-30 |
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10074590512189 | Consumable component for IPL6000 products |
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