Primary Device ID | 00817573023929 |
NIH Device Record Key | 2f0d18a0-9ac7-46ea-a421-6a53bcc1a6f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Equa-Pull |
Version Model Number | 830-212 |
Company DUNS | 045545589 |
Company Name | LANCER ORTHODONTICS, 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 | false |
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 |