Primary Device ID | 10884450007942 |
NIH Device Record Key | ce3a166a-7008-4f9d-9ac7-14a96d90467a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Revolution™ |
Version Model Number | 00884450007945 |
Catalog Number | CFG624/D |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00884450007945 [Primary] |
GS1 | 10884450007942 [Package] Contains: 00884450007945 Package: [25 Units] In Commercial Distribution |
KMK | DEVICE, INTRAVASCULAR CATHETER SECUREMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-02-16 |
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