Primary Device ID | 04952195089413 |
NIH Device Record Key | 75e8b7c2-acc8-464f-8940-3f1de33774b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Quolis 5000 Series Dental Unit |
Version Model Number | AU-BDS5180 |
Catalog Number | AU-BDS5180 |
Company DUNS | 690540349 |
Company Name | TAKARA-BELMONT CO., LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 |