Primary Device ID | 00816132022830 |
NIH Device Record Key | e0b4e97f-a902-4448-aa4d-a703f55842b2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Be Girl |
Version Model Number | Model 1 Standard |
Company DUNS | 604286695 |
Company Name | CASCO BAY MOLDING LTD. |
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 | false |
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 | 00816132022830 [Primary] |
HHE | Cup, Menstrual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-05 |
Device Publish Date | 2020-09-25 |
00850004683477 - Casco Cup | 2024-02-27 |
00850004683484 - Casco Cup | 2024-02-27 |
00850004683491 - Casco Cup | 2024-02-27 |
00850004683507 - Casco Cup | 2024-02-27 |
00850004683538 - Casco Cup | 2024-02-27 |
00850004683545 - Casco Cup | 2024-02-27 |
00850004683552 - Casco Cup | 2024-02-27 |
00850004683569 - Casco Cup | 2024-02-27 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BE GIRL 86559069 5046369 Live/Registered |
Be Girl, Inc. 2015-03-10 |