Primary Device ID | 00841013119132 |
NIH Device Record Key | 278fa53e-8244-4bef-b8b8-d1442b30e3e1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | American Eagle Instruments |
Version Model Number | MG3-4Z |
Company DUNS | 790776850 |
Company Name | AMERICAN EAGLE INSTRUMENTS, 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841013119132 [Primary] |
EMS | CURETTE, PERIODONTIC |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-31 |
Device Publish Date | 2022-05-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AMERICAN EAGLE INSTRUMENTS 86376282 4746794 Live/Registered |
AMERICAN EAGLE INSTRUMENTS, LLC 2014-08-25 |
AMERICAN EAGLE INSTRUMENTS 86115642 4559849 Live/Registered |
AMERICAN EAGLE INSTRUMENTS, LLC 2013-11-11 |
AMERICAN EAGLE INSTRUMENTS 74460271 1866874 Dead/Cancelled |
American Eagle Instruments, Inc. 1993-11-18 |