Primary Device ID | 00883205022080 |
NIH Device Record Key | c60c912e-0d58-413e-b740-a0e11e699c9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Micro 20 Gauge Tip |
Version Model Number | 1252 |
Catalog Number | 1252 |
Company DUNS | 013369913 |
Company Name | ULTRADENT PRODUCTS, INC. |
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 | true |
Serial Number | false |
Manufacturing Date | false |
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 |