Primary Device ID | 00817076014370 |
NIH Device Record Key | 9a4be58f-7082-4705-834e-62a157b7fbb0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | myCare |
Version Model Number | MF-94 |
Company DUNS | 121167779 |
Company Name | MICRO CURRENT 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 | 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 | 00817076014370 [Primary] |
NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-22 |
Device Publish Date | 2024-08-14 |
00817076014370 - myCare | 2024-08-22 |
00817076014370 - myCare | 2024-08-22 |
00817076014219 - bt-sculpt | 2024-03-07 |
00817076010952 - bt-degree | 2020-05-25 IR Thermometer |
00817076010877 - Bio- Ultimate Platinum | 2019-10-23 |
00817076010884 - bt-nano | 2019-10-23 |
00817076010822 - AutoCare | 2019-10-23 |
00817076010839 - HomeCare | 2019-10-23 |
00817076010846 - CustomCare | 2019-10-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MYCARE 87540709 5426703 Live/Registered |
Livell Company 2017-07-24 |
MYCARE 86738106 5106088 Live/Registered |
ONPOINT GROUP, LLC 2015-08-26 |
MYCARE 79233221 5790233 Live/Registered |
Signify Holding B.V. 2018-04-04 |
MYCARE 78414208 3099054 Live/Registered |
Gundersen Lutheran Administrative Services, Inc. 2004-05-06 |
MYCARE 75660335 not registered Dead/Abandoned |
Caresoft, Inc. 1999-03-15 |