Primary Device ID | 09369998146796 |
NIH Device Record Key | f2931945-85b5-4945-9009-2c9ca2a859a3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NervAlign Nerve Cuff |
Version Model Number | NA-NC2030 |
Catalog Number | NA-NC2030 |
Company DUNS | 744429508 |
Company Name | RENERVE 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 09369998146796 [Primary] |
JXI | Cuff, Nerve |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-18 |
Device Publish Date | 2022-04-08 |
09369998231904 | An absorbable collagen membrane implant that provides non-constricting protection for peripheral |
09369998146796 | An absorbable collagen membrane implant that provides non-constricting protection for peripheral |
09369998075812 | An absorbable collagen membrane implant that provides non-constricting protection for peripheral |