Primary Device ID | 10884450324810 |
NIH Device Record Key | c04b41a6-0379-428a-8c45-7cb851234011 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DiamondTOUCH™ |
Version Model Number | 00884450324813 |
Catalog Number | IN9403 |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
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 | 00884450324813 [Primary] |
GS1 | 10884450324810 [Package] Contains: 00884450324813 Package: [5 Units] In Commercial Distribution |
GS1 | 20884450324817 [Package] Package: [2 Units] In Commercial Distribution |
DXT | INJECTOR AND SYRINGE, ANGIOGRAPHIC |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2018-03-29 |
10884450324810 | 00884450324813 |
20884450324800 | 00884450324806 |
10884450324780 | 00884450324783 |
20884450264908 | 00884450264904 |
20884450413467 | 00884450413463 |
10884450409654 | 00884450409657 |
10884450409647 | 00884450409640 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DIAMONDTOUCH 87352328 5630343 Live/Registered |
Q.E.P. CO., INC. 2017-02-28 |