Primary Device ID | 10810027131499 |
NIH Device Record Key | 1fa45730-ec34-4793-8f1c-c6b2e3db7476 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rael |
Version Model Number | RAEL-CUP-MID1-V10-01 |
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 | 10810027131499 [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 | 2020-09-22 |
Device Publish Date | 2020-09-14 |
10810027131512 | Size 1 |
10810027131505 | Size 2 |
10810027131499 | Size 1 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RAEL 88827400 not registered Live/Pending |
Rael, Inc. 2020-03-09 |
RAEL 88540888 not registered Live/Pending |
Rael, Inc. 2019-07-26 |
RAEL 88494279 not registered Live/Pending |
Rael, Inc. 2019-06-28 |
RAEL 88312840 5845026 Live/Registered |
Rael, Inc. 2019-02-22 |
RAEL 88139664 not registered Live/Pending |
Rael, Inc. 2018-10-02 |
RAEL 87948859 not registered Live/Pending |
Rael, Inc. 2018-06-05 |
RAEL 87937110 not registered Live/Pending |
Rael, Inc. 2018-05-25 |
RAEL 87868531 not registered Live/Pending |
Cohen, Rael 2018-04-09 |
RAEL 87363909 5331785 Live/Registered |
RAEL, INC. 2017-03-08 |
RAEL 73701670 1530614 Dead/Cancelled |
ENIGMA, S.A. 1987-12-18 |
RAEL 73595396 1476251 Dead/Cancelled |
ENIGMA, S.A. 1986-04-24 |