Primary Device ID | 08800053070072 |
NIH Device Record Key | b557a428-bfe4-4da0-bf8e-0f801d1a320c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M300 Series (Ceiling, Mobile) |
Version Model Number | M300 |
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 | 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 | true |
OTC Over-The-Counter | false |