Primary Device ID | 00817051023632 |
NIH Device Record Key | 68bc2748-8a34-4d3f-b30f-246e202b6c67 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SilverSense |
Version Model Number | 310172 |
Company DUNS | 053707303 |
Company Name | CENTRIX, 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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |