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 |