Primary Device ID | 00811403017126 |
NIH Device Record Key | 14dc9d3e-eba5-4f9a-9915-257b32d7e9b3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sample Probe |
Version Model Number | OY-MU9934D |
Company DUNS | 947514303 |
Company Name | Diamond Diagnostics 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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |