Primary Device ID | 00869202000214 |
NIH Device Record Key | e5d6b69c-b7ab-4097-ba76-0a9226b5c1e6 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 9.0 |
Company DUNS | 152007423 |
Company Name | MEDHOST OF TENNESSEE, 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 | 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 |