| Primary Device ID | 00841013119347 |
| NIH Device Record Key | c93880c1-a82e-47b9-b621-9e9687752522 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | American Eagle Instruments |
| Version Model Number | MM17-18Z |
| 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 | 00841013119347 [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 |