Primary Device ID | 50023601220016 |
NIH Device Record Key | 63f8b1d9-7410-4bb8-ba1d-73f767dcef54 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AccuRelief |
Version Model Number | ACRL-2001 |
Company DUNS | 082522269 |
Company Name | Carex Health Brands |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 | 00023601220011 [Primary] |
GS1 | 30023601220012 [Package] Contains: 00023601220011 Package: PK [6 Units] In Commercial Distribution |
GS1 | 50023601220016 [Package] Contains: 30023601220012 Package: CA [6 Units] In Commercial Distribution |
NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2017-04-21 |
50023601290019 | AccuRelief Wireless Pain Relief Device |
50023601220016 | AccuRelief Single Channel Pain Relief Device |
00023601200013 | AccuRelief Universal Supply KIT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCURELIEF 86975656 4630018 Live/Registered |
COMPASS HEALTH BRANDS CORP. 2013-08-19 |
ACCURELIEF 86041329 not registered Dead/Abandoned |
Roscoe Medical, Inc. 2013-08-19 |