Primary Device ID | 09352307000865 |
NIH Device Record Key | cc0cffa4-4111-4ffd-a84d-5ac1fbd5fc44 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Evoke® Clarity™ Programming Application |
Version Model Number | 3044 |
Catalog Number | 3044 |
Company DUNS | 744596461 |
Company Name | SALUDA MEDICAL PTY LIMITED |
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 | false |
Manufacturing Date | false |
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 | 09352307000865 [Primary] |
LGW | Stimulator, Spinal-Cord, 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 | 2023-01-12 |
Device Publish Date | 2023-01-04 |