Primary Device ID | 00023601200013 |
NIH Device Record Key | a387c6de-f8f7-4187-8259-324764bf6552 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AccuRelief |
Version Model Number | ACRL-0001 |
Company DUNS | 082522269 |
Company Name | Carex Health Brands |
Device Count | 4 |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00023601200013 [Primary] |
GS1 | 01023601200017 [Unit of Use] |
GS1 | 30023601200014 [Package] Package: PK [6 Units] In Commercial Distribution |
GS1 | 50023601200018 [Package] Contains: 30023601200014 Package: CA [8 Units] In Commercial Distribution |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-02-19 |
Device Publish Date | 2016-10-05 |
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 |