InQwire® Amplatz IQA525
GUDID 10884450239695
Merit Medical Systems, Inc.
Cardiac/peripheral vascular guidewire, single-use| Primary Device ID | 10884450239695 |
| NIH Device Record Key | fe6fb3c9-5721-4b7d-a6b1-f95dac371e42 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InQwire® Amplatz |
| Version Model Number | 00884450239698 |
| Catalog Number | IQA525 |
| 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 | false |
| OTC Over-The-Counter | false |
Device Dimensions
| 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 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450239698 [Primary] |
| GS1 | 10884450239695 [Package] Contains: 00884450239698 Package: [5 Units] In Commercial Distribution |
| GS1 | 20884450239692 [Package] Package: [20 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K163575
FDA Product Code
| DQX | WIRE, GUIDE, CATHETER |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-04-06 |
On-Brand Devices [InQwire® Amplatz]
| 10884450355968 | 00884450355961 |
| 20884450355958 | 00884450355954 |
| 10884450335977 | 00884450335970 |
| 20884450311510 | 00884450311516 |
| 20884450311497 | 00884450311493 |
| 10884450239800 | 00884450239803 |
| 10884450239794 | 00884450239797 |
| 10884450239787 | 00884450239780 |
| 10884450239770 | 00884450239773 |
| 20884450239760 | 00884450239766 |
| 20884450239753 | 00884450239759 |
| 10884450239749 | 00884450239742 |
| 20884450239739 | 00884450239735 |
| 10884450239718 | 00884450239711 |
| 10884450239701 | 00884450239704 |
| 10884450239695 | 00884450239698 |
| 20884450239685 | 00884450239681 |
| 10884450239671 | 00884450239674 |
| 20884450239661 | 00884450239667 |
| 10884450239503 | 00884450239506 |
| 10884450239497 | 00884450239490 |
| 10884450239473 | 00884450239476 |
| 20884450239463 | 00884450239469 |
| 20884450239456 | 00884450239452 |
| 10884450434632 | 00884450434635 |
| 20884450434622 | 00884450434628 |
| 20884450434646 | 00884450434642 |
Trademark Results [InQwire]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INQWIRE 86803978 5092667 Live/Registered |
Nephew, Jill 2015-10-29 |
 INQWIRE 85794963 not registered Dead/Abandoned |
AROUNDWIRE, LLC 2012-12-05 |
 INQWIRE 75356437 2494586 Live/Registered |
Merit Medical Systems, Inc. 1997-08-22 |
 INQWIRE 75356352 2494585 Live/Registered |
Merit Medical Systems, Inc. 1997-08-22 |
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