Primary Device ID | 00667259001563 |
NIH Device Record Key | ddd0d7d9-34a5-4880-81de-c571d43bf5be |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ST250 |
Version Model Number | 411101 |
Company DUNS | 242049828 |
Company Name | Silhouet-Tone Corporation |
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 | false |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com | |
Phone | 1-866-340-9456 |
info@silhouettone.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00667259001563 [Primary] |
KCW | Epilator, High Frequency, Needle-Type |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-24 |
Device Publish Date | 2018-08-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ST250 75812677 not registered Dead/Abandoned |
K-Swiss Inc. 1999-09-30 |