Primary Device ID | B839B7RW9NMMV783BC3AA0 |
NIH Device Record Key | 66a3aff5-7c53-494c-8b84-bd597db7e282 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | myEverCup |
Version Model Number | 5D8415DSWB7RW9NMMV783BC3AA |
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 |
---|---|
HIBCC | B839B7RW9NMMV783BC3AA0 [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 | 2020-09-01 |
Device Publish Date | 2020-08-24 |
B8397QJMD6N2Q2171C34A0 | 7KTD9QAT57QJMD6N2Q2171C34A |
B839DMRNTRQE6EDADE6FB0 | 2ADMAN735DMRNTRQE6EDADE6FB |
B839CA7ZCG9YCAFA25EDA0 | 2AXHQMKBQCA7ZCG9YCAFA25EDA |
B839842F766HT2D0589630 | 3HQAZHE9N842F766HT2D058963 |
B8394F5BS5GTNE2FDC52C0 | 3PNGECWSA4F5BS5GTNE2FDC52C |
B839WBWANSWY6FPTX7PBP0 | 6QMAAWMW4WBWANSWY6FPTX7PBP |
B839NZXX6FYD9602885870 | 02BEK8T60NZXX6FYD960288587 |
B839KZ20F2N9PK2CS8B5H0 | 26X0ARWN1KZ20F2N9PK2CS8B5H |
B8390JNDAGCY2094980F40 | 4582RS8TV0JNDAGCY2094980F4 |
B839W6983X41NCA53893A0 | Size 1 Standard with Violet Cleaning Case |
B839B7RW9NMMV783BC3AA0 | Size 1 Standard with Orange Cleaning Case |