Primary Device ID | 20726893111954 |
NIH Device Record Key | e81cf120-3fcf-4c5d-a9ff-16c8b1c2ad9e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | One Vanish Hyperthin |
Version Model Number | 111308 |
Company DUNS | 364614362 |
Company Name | GLOBAL PROTECTION CORP. |
Device Count | 40 |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00726893111950 [Primary] |
GS1 | 20726893111954 [Package] Contains: 00726893111950 Package: 24 of 40 count pack [24 Units] In Commercial Distribution |
GS1 | 80726893111307 [Unit of Use] |
HIS | Condom |
QRZ | External Condom For Anal Intercourse Or Vaginal Intercourse |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-06-23 |
Device Publish Date | 2020-06-15 |
20726893111954 | Male Lubricated Latex Condoms |
10726893111308 | Lubricated Male Latex Condoms |
80726893114674 | Latex Lubricated Condoms |