Primary Device ID | 08800053083898 |
NIH Device Record Key | 13b9788c-af0e-4ce4-a6b1-6b492b1803d5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LUVIS-C300 Series |
Version Model Number | C300 CEILING |
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 |