Primary Device ID | 00022600001119 |
NIH Device Record Key | a033f64d-2047-4783-800a-3ddc229906e3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RepHresh™ Vaginal Gel Personal Lubricant |
Version Model Number | 00022600001119 |
Company DUNS | 001211952 |
Company Name | CHURCH & DWIGHT CO., INC. |
Device Count | 4 |
DM Exempt | true |
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 | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00022600001119 [Primary] |
GS1 | 80022600001115 [Unit of Use] |
NUC | Lubricant, personal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-08-07 |
Device Publish Date | 2016-10-14 |
00022600987628 | 00022600987628 |
00022600019657 | 00022600019657 |
00022600001119 | 00022600001119 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
REPHRESH 90628991 not registered Live/Pending |
Restore RX Beauty LLC 2021-04-07 |
REPHRESH 87710628 not registered Live/Pending |
CHURCH & DWIGHT CO., INC. 2017-12-06 |
REPHRESH 79316315 not registered Live/Pending |
LIN Xijian 2021-04-20 |
REPHRESH 78912034 not registered Dead/Abandoned |
Hikari Holdings, L.C. 2006-06-20 |
REPHRESH 77065321 3591790 Live/Registered |
CHURCH & DWIGHT CO., INC. 2006-12-15 |
REPHRESH 76317240 2757069 Live/Registered |
CHURCH & DWIGHT CO., INC. 2001-09-26 |