Primary Device ID | 08806169147943 |
NIH Device Record Key | 9955972c-4e80-45a4-bea5-6dbc2ca19b6f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M300 Series (ceiling, Mobile) |
Version Model Number | M310 |
Company DUNS | 694721181 |
Company Name | DENTIS CO. ,LTD |
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 | false |
Device Combination Product | false |
Single Use | true |
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 |