Primary Device ID | 20884450390737 |
NIH Device Record Key | 31ac8dcf-48c2-4993-9f86-538c6971e027 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DualCap® |
Version Model Number | 10884450390730 |
Catalog Number | 500-LB/B |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 350 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 00884450390733 [Unit of Use] |
GS1 | 10884450390730 [Primary] |
GS1 | 20884450390737 [Package] Contains: 10884450390730 Package: [12 Units] In Commercial Distribution |
LKB | Pad, alcohol, device disinfectant |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-08-07 |
Device Publish Date | 2018-09-24 |
20884450309456 | 10884450309459 |
20884450390737 | 10884450390730 |
20884450309425 | 10884450309428 |
20884450309418 | 10884450309411 |
20884450309371 | 10884450309374 |
20884450309364 | 10884450309367 |
20884450309975 | 10884450309978 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DUALCAP 77705452 4023166 Live/Registered |
MERIT MEDICAL SYSTEMS, INC. 2009-04-02 |