Primary Device ID | 10884450275624 |
NIH Device Record Key | ba8e1351-09a7-4465-b37d-c401a33ea4f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Merit PAK™ |
Version Model Number | 00884450275627 |
Catalog Number | PAKM4NPD4/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 |
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Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450275627 [Primary] |
GS1 | 10884450275624 [Package] Contains: 00884450275627 Package: [5 Units] In Commercial Distribution |
DRE | DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION |
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 | 2018-01-09 |
10884450275716 | 00884450275719 |
10884450275693 | 00884450275696 |
10884450275624 | 00884450275627 |
10884450275686 | 00884450275689 |
10884450275662 | 00884450275665 |
10884450275723 | 00884450275726 |
10884450275730 | 00884450275733 |
20884450275577 | 10884450275570 |
20884450275560 | 10884450275563 |
10884450587130 | 00884450587133 |
10884450587147 | 00884450587140 |
10884450587123 | 00884450587126 |
10884450587192 | 00884450587195 |
10884450587178 | 00884450587171 |
10884450587154 | 00884450587157 |
10884450587161 | 00884450587164 |