Primary Device ID | 20884450518285 |
NIH Device Record Key | aa612c15-fc7a-4b33-aaf8-2efdad399f88 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prelude IDeal™ |
Version Model Number | 10884450518288 |
Catalog Number | PID7F23021PW/B |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00884450518281 [Unit of Use] |
GS1 | 10884450518288 [Primary] |
GS1 | 20884450518285 [Package] Contains: 10884450518288 Package: [4 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 | 2021-02-04 |
Device Publish Date | 2021-01-27 |
20884450317543 | 10884450317546 |
20884450317741 | 10884450317744 |
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20884450335028 | 10884450335021 |
20884450335004 | 10884450335007 |
20884450334991 | 10884450334994 |
20884450320468 | 10884450320461 |
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20884450317215 | 10884450317218 |