Primary Device ID | 10884450313319 |
NIH Device Record Key | a65e1497-ce0e-4d6b-a7f2-7178f4ef23e9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Prelude Prestige™ |
Version Model Number | 10884450313319 |
Catalog Number | PLP-1005 |
Company DUNS | 065673912 |
Company Name | Merit Medical |
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 | 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 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 | 00884450313312 [Unit of Use] |
GS1 | 10884450313319 [Primary] |
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 | 2019-06-17 |
Device Publish Date | 2019-06-07 |
10884450313883 | 10884450313883 |
10884450313517 | 10884450313517 |
10884450313487 | 10884450313487 |
10884450313470 | 10884450313470 |
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10884450313463 | 10884450313463 |
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10884450313395 | 10884450313395 |
10884450313388 | 10884450313388 |
10884450313326 | 10884450313326 |
10884450313319 | 10884450313319 |
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00884450313732 | 10884450313739 |
00884450313794 | 10884450313791 |
00884450313763 | 10884450313760 |