Primary Device ID | 07350120790538 |
NIH Device Record Key | 80fb755d-54ed-4909-ab1f-b3da39e7d0f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ESPADA 2 |
Version Model Number | Cobalt Blue |
Company DUNS | 352394143 |
Company Name | Foreo AB |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07350120790538 [Primary] |
OLP | Over-The-Counter Powered Light Based Laser For Acne |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-14 |
Device Publish Date | 2024-08-06 |
07350120791771 | The ESPADA 2 Acne-Clearing Blue Light Pen is intended for use as an at-home device for the treat |
07350120790538 | The ESPADA 2 Acne-Clearing Blue Light Pen is intended for use as an at-home device for the treat |
07350120790521 | The ESPADA 2 Acne-Clearing Blue Light Pen is intended for use as an at-home device for the treat |