Primary Device ID | 10884450414757 |
NIH Device Record Key | fb4b008a-efc0-4dbb-b237-dd11f2eeb696 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ReSolve®, Revolution™ |
Version Model Number | 00884450414750 |
Catalog Number | RBC-14-REV/A |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00884450414750 [Primary] |
GS1 | 10884450414757 [Package] Contains: 00884450414750 Package: [5 Units] In Commercial Distribution |
FGE | Stents, drains and dilators for the biliary ducts |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-03 |
Device Publish Date | 2021-04-23 |
10884450086022 | 00884450086025 |
10884450057480 | 00884450057483 |
10884450030063 | 00884450030066 |
10884450026127 | 00884450026120 |
10884450026110 | 00884450026113 |
10884450023829 | 00884450023822 |
10884450022969 | 00884450022962 |
10884450022235 | 00884450022238 |
10884450022204 | 00884450022207 |
10884450019792 | 00884450019795 |
10884450086039 | 00884450086032 |
10884450414757 | 00884450414750 |
10884450057831 | 00884450057834 |
10884450076702 | 00884450076705 |