| Primary Device ID | 20888937000027 |
| NIH Device Record Key | da942d3c-220d-4bac-bbab-7194211fc06a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Her Option |
| Version Model Number | CU-1 |
| Company DUNS | 801895244 |
| Company Name | Coopersurgical, 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20888937000027 [Primary] |
| MNB | Device, Thermal Ablation, Endometrial |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-17 |
| 20888937000027 | Her Option Disposable Probe |
| 00888937000016 | Her Option Console |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HER OPTION 90877126 not registered Live/Pending |
Glenmark Therapeutics Inc., USA 2021-08-11 |
![]() HER OPTION 76233579 2711926 Live/Registered |
COOPERSURGICAL INC. 2001-03-30 |