Primary Device ID | 00850470007517 |
NIH Device Record Key | 38280d8a-8145-4752-9e81-b174efb14564 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Disposable Kits, Sterile and Non-Sterile (S) |
Version Model Number | 20G 4 Prong |
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 | 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 |