Primary Device ID | 05391527770626 |
NIH Device Record Key | e80e17ab-a1da-40b1-93c1-0716c0e1c9b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ReActiv8 Magnet |
Version Model Number | 6M4000-003 |
Catalog Number | 4000 |
Company DUNS | 985519015 |
Company Name | MAINSTAY MEDICAL LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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 | 05391527770626 [Primary] |
QLK | Stimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain Relief |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-02-02 |
Device Publish Date | 2021-01-25 |
05391527770633 | ReActiv8 Magnet (for use in starting or stopping therapy dependent upon IPG programming). |
05391527770626 | ReActiv8 Magnet (for use in starting or stopping therapy dependent upon IPG programming). |