Primary Device ID | E241VI0010 |
NIH Device Record Key | be508fdc-df55-4b83-8358-95c15b3db031 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cavex Vibringe |
Version Model Number | VI001 |
Catalog Number | VI001 |
Company DUNS | 419980156 |
Company Name | Cavex Holland B.V. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |