Primary Device ID | B521108832120212 |
NIH Device Record Key | 5ce3bd86-b056-4588-9553-b147f66b1490 |
Commercial Distribution Discontinuation | 2019-02-01 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ECHO XL TiNano OLIF |
Version Model Number | 108032120212 |
Catalog Number | 108832120212 |
Company DUNS | 079119091 |
Company Name | AURORA SPINE, INC. |
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 |