Primary Device ID | 00858711006367 |
NIH Device Record Key | af9e6a2f-40d4-4b56-8105-12756abeba34 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AuraPrene |
Version Model Number | DDS-303 |
Catalog Number | DDS-303 |
Company DUNS | 018638145 |
Company Name | AMERICAN MEDICAL & DENTAL SUPPLIES INC |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |