Primary Device ID | 00718175087626 |
NIH Device Record Key | 30bd866b-19a2-4dba-8627-2dc5108e0f06 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VENTI-SCAN IV |
Version Model Number | 177-090 |
Catalog Number | 177-090 |
Company DUNS | 043833813 |
Company Name | BIODEX MEDICAL SYSTEMS, 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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 |