| Primary Device ID | 10884450836030 |
| NIH Device Record Key | 08dce2da-60ed-40d2-8eee-faf9e2f2f3fb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Performa® |
| Version Model Number | D |
| Catalog Number | 5RPS125-NB |
| 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 Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450836033 [Primary] |
| GS1 | 10884450836030 [Package] Contains: 00884450836033 Package: [5 Units] In Commercial Distribution |
| DQO | Catheter, intravascular, diagnostic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-10-02 |
| Device Publish Date | 2025-09-24 |
| 10884450408589 | 00884450408582 |
| 10884450408572 | 00884450408575 |
| 10884450394745 | 00884450394748 |
| 10884450394721 | 00884450394724 |
| 10884450383411 | 00884450383414 |
| 10884450383404 | 00884450383407 |
| 10884450363116 | 00884450363119 |
| 10884450362942 | 00884450362945 |
| 10884450362843 | 00884450362846 |
| 10884450362836 | 00884450362839 |
| 10884450362829 | 00884450362822 |
| 10884450362805 | 00884450362808 |
| 10884450362645 | 00884450362648 |
| 10884450362638 | 00884450362631 |
| 10884450362621 | 00884450362624 |
| 10884450362577 | 00884450362570 |
| 10884450362560 | 00884450362563 |
| 10884450362553 | 00884450362556 |
| 10884450362546 | 00884450362549 |
| 10884450362225 | 00884450362228 |
| 10884450362218 | 00884450362211 |
| 10884450362195 | 00884450362198 |
| 10884450362188 | 00884450362181 |
| 10884450362164 | 00884450362167 |
| 10884450362157 | 00884450362150 |
| 10884450362102 | 00884450362105 |
| 10884450362096 | 00884450362099 |
| 10884450362089 | 00884450362082 |
| 10884450362065 | 00884450362068 |
| 10884450362041 | 00884450362044 |
| 10884450362027 | 00884450362020 |
| 10884450362003 | 00884450362006 |
| 10884450360931 | 00884450360934 |
| 10884450358877 | 00884450358870 |
| 10884450356675 | 00884450356678 |
| 10884450356606 | 00884450356609 |
| 10884450356590 | 00884450356593 |
| 10884450356583 | 00884450356586 |
| 10884450356576 | 00884450356579 |
| 10884450356569 | 00884450356562 |
| 10884450356552 | 00884450356555 |
| 10884450320751 | 00884450320754 |
| 10884450320744 | 00884450320747 |
| 10884450320737 | 00884450320730 |
| 10884450320720 | 00884450320723 |
| 10884450314798 | 00884450314791 |
| 10884450309602 | 00884450309605 |
| 10884450307004 | 00884450307007 |
| 10884450306977 | 00884450306970 |
| 10884450306823 | 00884450306826 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PERFORMA 98355199 not registered Live/Pending |
Colson Group USA, LLC 2024-01-12 |
![]() PERFORMA 98128394 not registered Live/Pending |
Gerdau Macsteel, Inc. 2023-08-11 |
![]() PERFORMA 90723564 not registered Live/Pending |
ARCESIUM LLC 2021-05-20 |
![]() PERFORMA 88734959 not registered Live/Pending |
Quadratec, Inc. 2019-12-20 |
![]() PERFORMA 88663369 not registered Live/Pending |
Reece Australia Pty Ltd 2019-10-22 |
![]() PERFORMA 88354438 not registered Live/Pending |
ENERGIZER AUTO, INC. 2019-03-25 |
![]() PERFORMA 88095900 not registered Dead/Abandoned |
AS IP Holdco, LLC 2018-08-28 |
![]() PERFORMA 88004914 5679143 Live/Registered |
Perfoma Limited (US) LLC 2018-06-18 |
![]() PERFORMA 87570253 not registered Live/Pending |
Cyrus Creations LLC 2017-08-15 |
![]() PERFORMA 87551203 not registered Live/Pending |
1535674 Alberta, Inc. 2017-08-01 |
![]() PERFORMA 87457413 not registered Dead/Abandoned |
Vytalyx Inc 2017-05-19 |
![]() PERFORMA 87379635 5461970 Live/Registered |
Performance Health Holdings, Inc. 2017-03-21 |