Primary Device ID | B839Q4CJQDNSYF2B59D130 |
NIH Device Record Key | e85aff75-de1f-4856-93d6-9155133d18b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Venus Cup |
Version Model Number | S |
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 |