Primary Device ID | 10884450076030 |
NIH Device Record Key | d5161294-2c77-4b6a-8715-4d1ca4bd56d6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Softouch® |
Version Model Number | 00884450076033 |
Catalog Number | 1628-55 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450076033 [Primary] |
GS1 | 10884450076030 [Package] Contains: 00884450076033 Package: [5 Units] In Commercial Distribution |
DQO | CATHETER, INTRAVASCULAR, DIAGNOSTIC |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
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