InQwire® IQ38F150S/B
GUDID 20884450005129
Merit Medical Systems, Inc.
Cardiac/peripheral vascular guidewire, single-use| Primary Device ID | 20884450005129 |
| NIH Device Record Key | 1ed0838e-b798-49ec-83c4-ef514a20cac9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InQwire® |
| Version Model Number | 00884450005125 |
| Catalog Number | IQ38F150S/B |
| 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 | 00884450005125 [Primary] |
| GS1 | 10884450005122 [Package] Contains: 00884450005125 Package: [10 Units] In Commercial Distribution |
| GS1 | 20884450005129 [Package] Contains: 10884450005122 Package: [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K133230
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 | 2016-09-24 |
On-Brand Devices [InQwire®]
| 20884450327801 | 00884450327807 |
| 10884450268145 | 00884450268148 |
| 20884450261143 | 00884450261149 |
| 20884450251465 | 00884450251461 |
| 10884450243623 | 00884450243626 |
| 10884450233839 | 00884450233832 |
| 10884450231897 | 00884450231890 |
| 20884450199392 | 00884450199398 |
| 20884450198821 | 00884450198827 |
| 10884450198626 | 00884450198629 |
| 20884450196384 | 00884450196380 |
| 10884450196370 | 00884450196373 |
| 10884450196363 | 00884450196366 |
| 10884450151553 | 00884450151556 |
| 20884450094604 | 00884450094600 |
| 10884450094478 | 00884450094471 |
| 10884450085315 | 00884450085318 |
| 10884450081188 | 00884450081181 |
| 10884450072131 | 00884450072134 |
| 10884450058524 | 00884450058527 |
| 10884450057602 | 00884450057605 |
| 10884450057046 | 00884450057049 |
| 20884450056800 | 00884450056806 |
| 10884450056797 | 00884450056790 |
| 20884450056787 | 00884450056783 |
| 10884450056759 | 00884450056752 |
| 20884450056749 | 00884450056745 |
| 10884450056575 | 00884450056578 |
| 10884450056537 | 00884450056530 |
| 20884450056503 | 00884450056509 |
| 10884450056391 | 00884450056394 |
| 20884450056381 | 00884450056387 |
| 20884450056374 | 00884450056370 |
| 10884450056360 | 00884450056363 |
| 20884450056350 | 00884450056356 |
| 10884450056346 | 00884450056349 |
| 20884450056299 | 00884450056295 |
| 10884450056254 | 00884450056257 |
| 10884450046224 | 00884450046227 |
| 20884450044081 | 00884450044087 |
| 10884450044077 | 00884450044070 |
| 10884450044060 | 00884450044063 |
| 00884450044032 | 00884450044032 |
| 00884450044018 | 00884450044018 |
| 00884450044001 | 00884450044001 |
| 10884450029937 | 00884450029930 |
| 10884450029913 | 00884450029916 |
| 10884450029906 | 00884450029909 |
| 20884450029255 | 00884450029251 |
| 20884450029248 | 00884450029244 |
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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