| Primary Device ID | 00197644645664 |
| NIH Device Record Key | 077222ec-cb63-40f9-965a-ec40fb36c068 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Humes |
| Version Model Number | Size 2 |
| 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 | 00197644645664 [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 | 2023-06-14 |
| Device Publish Date | 2023-06-06 |
| 00197644760619 | Disc |
| 00197644645664 | Size 2 |
| 00197644014033 | Size 1 |
| 00860011787327 | Disc |
| 00860011787310 | Size 2 |
| 00860011787303 | Size 1 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HUMES 73642935 1525008 Dead/Cancelled |
HUMES LIMITED 1987-02-04 |