| 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 |