Primary Device ID | 00850470007241 |
NIH Device Record Key | 8ddc8b09-0918-4fe9-8020-cba8a5f77229 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reusable Kit |
Version Model Number | Site Making |
Catalog Number | FP-46446 |
Company DUNS | 627212587 |
Company Name | RESTORATION ROBOTICS, 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 | false |
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 |