| Primary Device ID | 10884450433079 |
| NIH Device Record Key | 7b248266-8098-48c3-8d23-e1f2c899aa1d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Merit Medical® |
| Version Model Number | 00884450433072 |
| Catalog Number | MIS-099-00/A |
| Company DUNS | 065673912 |
| Company Name | Merit Medical |
| Device Count | 1 |
| 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 | true |
| 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 | 00884450433072 [Primary] |
| GS1 | 10884450433079 [Package] Contains: 00884450433072 Package: [5 Units] In Commercial Distribution |
| GS1 | 20884450433076 [Package] Package: [12 Units] In Commercial Distribution |
| DWS | INSTRUMENTS, SURGICAL, CARDIOVASCULAR |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-04-14 |
| Device Publish Date | 2020-04-06 |
| 00884450164631 | 00884450164631 |
| 10884450164621 | 00884450164624 |
| 10884450433079 | 00884450433072 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MERIT MEDICAL 86670250 5548106 Live/Registered |
Merit Medical Systems, Inc. 2015-06-22 |
![]() MERIT MEDICAL 85801215 4413590 Live/Registered |
Merit Medical Systems, Inc. 2012-12-12 |