Primary Device ID | 00851640007405 |
NIH Device Record Key | 05ea2f35-ddf8-4dc5-807b-0538c1f4b71e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PRO-TECH |
Version Model Number | HD-5N-N |
Company DUNS | 124034476 |
Company Name | Hi-Dow International Incorporated |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851640007405 [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 | 4 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2017-09-27 |
00851640007405 | Pro-Tech Wireless |
00851640007238 | MICRO-TECH |
00851640007221 | SMART-TECH |
00851640007214 | PRO-TECH Massager |