Primary Device ID | 00811403017089 |
NIH Device Record Key | 303af46e-cdcc-4b6d-8cac-a295c7c836e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reference Electrode |
Version Model Number | OY-MU9197D |
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 | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |