Primary Device ID | 08800053083966 |
NIH Device Record Key | d79683ac-1348-4ab9-a194-a4b5a97c07f1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LUVIS-C500 Series |
Version Model Number | C500 WALL |
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 |