Primary Device ID | 00761236110160 |
NIH Device Record Key | fe301a44-5f3c-47e1-81aa-07ab145acedc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ID Condoms |
Version Model Number | ID Condoms Assorted Jar |
Catalog Number | IDDCASJ0 |
Company DUNS | 879057065 |
Company Name | WESTRIDGE LABORATORIES INCORPORATED |
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 | true |
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 |
Phone | 7142599400 |
service@westridgelabs.com | |
Phone | 7142599400 |
service@westridgelabs.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00761236110160 [Primary] |
HIS | Condom |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-05-03 |
60761236901128 | A premium lubricated latex condom |
00761236901119 | A premium lubricated latex condom |
60761236901098 | Premium lubricated Latex Condom |
60761236901074 | Premium lubricated Latex Condom |
00761236110290 | A premium lubricated latex condom |
00761236110276 | A premium lubricated latex condom |
00761236110269 | A premium lubricated latex condom |
00761236110245 | A premium lubricated latex condom |
00761236110238 | Premium lubricated Latex Condom |
00761236110214 | Premium lubricated Latex Condom |
00761236110207 | Premium lubricated Latex Condom |
00761236110184 | Premium lubricated Latex Condom |
00761236110160 | An assortment of the ID Condom lines [ID Superior Feel, ID Studded, ID Extra Thin, and ID Extra |