Primary Device ID | 00816305023275 |
NIH Device Record Key | 3bf3bc70-92ed-49a3-8815-93fe4d923ed6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flexitouch |
Version Model Number | DS WX-L |
Company DUNS | 146295980 |
Company Name | TACTILE SYSTEMS TECHNOLOGY, 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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816305023275 [Primary] |
JOW | Sleeve, Limb, Compressible |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-05-04 |
Device Publish Date | 2017-10-27 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLEXITOUCH 78525094 3134191 Live/Registered |
TACTILE SYSTEMS TECHNOLOGY, INC. 2004-12-01 |
FLEXITOUCH 78156230 2765826 Live/Registered |
TACTILE SYSTEMS TECHNOLOGY, INC. 2002-08-21 |