| Primary Device ID | 10884450838362 |
| NIH Device Record Key | ecf65b60-b768-4e5d-a2cc-836d5a8998ac |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Abiomed® |
| Version Model Number | 00884450838365 |
| Catalog Number | 1000440 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450838365 [Primary] |
| GS1 | 10884450838362 [Package] Contains: 00884450838365 Package: [5 Units] In Commercial Distribution |
| DYB | Introducer, catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-09 |
| Device Publish Date | 2025-07-01 |
| 10884450732318 | 00884450732311 |
| 10884450838362 | 00884450838365 |
| 00884450101667 | 10884450101664 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ABIOMED 98112899 not registered Live/Pending |
Amnio Technology LLC 2023-08-02 |
![]() ABIOMED 77211222 3439485 Live/Registered |
ABIOMED, Inc. 2007-06-20 |
![]() ABIOMED 77211209 3474929 Live/Registered |
ABIOMED, Inc. 2007-06-20 |
![]() ABIOMED 77211203 3439484 Live/Registered |
ABIOMED, Inc. 2007-06-20 |
![]() ABIOMED 74068233 1645900 Live/Registered |
Abiomed, Inc. 1990-06-12 |
![]() ABIOMED 73454060 1332596 Live/Registered |
Applied Biomedical Corporation 1983-11-23 |