Primary Device ID | 00850002174557 |
NIH Device Record Key | 92dea99d-1a75-4556-84c5-d9aa088d4bbf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Beyond Seven |
Version Model Number | GS182 |
Company DUNS | 106855461 |
Company Name | LUNAMAX LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850002174557 [Primary] |
HIS | Condom |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-12-28 |
Device Publish Date | 2018-11-27 |
00850002174564 | Beyond Seven Mega Big Boy Latex Condom |
00850002174557 | Beyond Seven Mega Big Boy Latex Condom |
00850002174540 | Beyond Seven Ribbed Latex Condom |
00850002174533 | Beyond Seven Ribbed Latex Condom |
00850002174526 | Beyond Seven Ultra Thin Latex Condom |
00850002174519 | Beyond Seven Ultra Thin Latex Condom |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BEYOND SEVEN 74193853 1707955 Live/Registered |
OKAMOTO U.S.A., INC. 1991-08-12 |