Primary Device ID | 15420045500969 |
NIH Device Record Key | adc28f87-0822-4006-a4a4-9b7ae7664343 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cervista HTA System |
Version Model Number | Cervista HTA System |
Company DUNS | 018925968 |
Company Name | Hologic, Inc. |
Device Count | 1 |
DM Exempt | true |
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 | 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 | false |