Primary Device ID | 00840001700055 |
NIH Device Record Key | 40b6fe33-c3db-4040-aabf-819d9ff3d2ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ulaif |
Version Model Number | R-T1 |
Company DUNS | 544587118 |
Company Name | Shenzhen roundwhale technology co. LTD. |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 00840001700055 [Primary] |
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 | 3 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2018-07-16 |
00840001700055 | It is used for temporary relief of pain associated with sore and aching muscles in the shoulder, |
00840001700048 | It is used for temporary relief of pain associated with sore and aching muscles in the shoulder, |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ULAIF 87736183 5529829 Live/Registered |
Beijing Mo Xing Tian Xia Mo Xing Ke Ji You Xian Gong Si 2017-12-28 |