Primary Device ID | 00190746153495 |
NIH Device Record Key | 683636c4-726e-4cb3-b6c9-0aa960557713 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ceramic Button |
Version Model Number | 855-032459 |
Catalog Number | 855-032459 |
Company DUNS | 044668515 |
Company Name | AMERICAN ORTHODONTICS CORPORATION |
Device Count | 1 |
DM Exempt | true |
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 | 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 |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com | |
Phone | +1(800)558-7687 |
info@americanortho.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190746153495 [Primary] |
ECN | CLAMP, WIRE, ORTHODONTIC |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-01 |
Device Publish Date | 2024-03-22 |
00190746074301 | DB CERAMIC BUTTON 10/PKG |
00190746153495 | DB CERAMIC BUTTON 10/PK |