Primary Device ID | 20884450331822 |
NIH Device Record Key | 6e2ac693-2d62-4033-838e-a509c108c84d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prelude® |
Version Model Number | 10884450331825 |
Catalog Number | PSI-7F-11/C |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 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 | 00884450331828 [Unit of Use] |
GS1 | 10884450331825 [Primary] |
GS1 | 20884450331822 [Package] Contains: 10884450331825 Package: [4 Units] In Commercial Distribution |
DRE | DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-06-07 |
Device Publish Date | 2018-03-05 |
20884450332027 | 10884450332020 |
20884450331587 | 10884450331580 |
20884450331877 | 10884450331870 |
20884450332034 | 10884450332037 |
20884450331969 | 10884450331962 |
20884450331952 | 10884450331955 |
20884450331945 | 10884450331948 |
20884450331921 | 10884450331924 |
20884450331907 | 10884450331900 |
20884450331860 | 10884450331863 |
20884450331853 | 10884450331856 |
20884450331846 | 10884450331849 |
20884450331822 | 10884450331825 |
20884450331808 | 10884450331801 |
20884450331723 | 10884450331726 |
20884450331655 | 10884450331658 |
20884450331648 | 10884450331641 |
20884450331631 | 10884450331634 |
20884450331617 | 10884450331610 |
20884450331594 | 10884450331597 |
20884450331556 | 10884450331559 |
20884450331532 | 10884450331535 |
20884450331518 | 10884450331511 |
20884450331327 | 10884450331320 |
20884450331273 | 10884450331276 |
20884450331266 | 10884450331269 |
20884450331211 | 10884450331214 |
20884450331204 | 10884450331207 |
20884450330696 | 10884450330699 |
20884450330665 | 10884450330668 |
20884450330641 | 10884450330644 |
20884450330610 | 10884450330613 |
20884450330597 | 10884450330590 |
20884450330573 | 10884450330576 |
20884450330566 | 10884450330569 |
20884450330528 | 10884450330521 |
20884450330504 | 10884450330507 |
20884450330467 | 10884450330460 |
20884450292444 | 10884450292447 |
20884450292437 | 10884450292430 |
20884450199330 | 10884450199333 |
20884450123809 | 10884450123802 |
20884450081529 | 10884450081522 |
20884450057821 | 10884450057824 |
20884450019775 | 10884450019778 |
20884450011366 | 10884450011369 |
20884450010659 | 10884450010652 |
20884450010628 | 10884450010621 |
20884450010512 | 10884450010515 |
20884450009806 | 10884450009809 |
Mark Image Registration | Serial | Company Trademark Application Date |
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DING 2024-10-31 |
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