Primary Device ID | 00894912002036 |
NIH Device Record Key | 365912d0-8bf1-4218-bb23-f0482f249f83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CT |
Version Model Number | CT-4 |
Catalog Number | CT-4 |
Company DUNS | 069261402 |
Company Name | KOVEN TECHNOLOGY, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 | false |