Primary Device ID | 00024291262800 |
NIH Device Record Key | 229d9026-7ba2-4353-b559-b66bbdb67f31 |
Commercial Distribution Discontinuation | 2021-02-10 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Handy Solutions |
Version Model Number | 26103 |
Company DUNS | 091917799 |
Company Name | Navajo Manufacturing Company |
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 | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00024291262800 [Primary] |
HIS | Condom |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-07-13 |
Device Publish Date | 2016-08-31 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HANDY SOLUTIONS 86195717 4853555 Live/Registered |
Navajo Manufacturing Company 2014-02-17 |
HANDY SOLUTIONS 75718324 2440062 Live/Registered |
NAVAJO MANUFACTURING CO. 1999-06-01 |