Primary Device ID | 10886333214294 |
NIH Device Record Key | 8646b40f-23bc-47c2-a956-176c364ca8f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hemostasis Valve 4F-6F |
Version Model Number | 497296 |
Catalog Number | 497296 |
Company DUNS | 140727624 |
Company Name | ARGON MEDICAL DEVICES, 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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com | |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886333214297 [Primary] |
GS1 | 10886333214294 [Package] Contains: 00886333214297 Package: Box [10 Units] In Commercial Distribution |
GS1 | 20886333214291 [Package] Contains: 00886333214297 Package: Box [40 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 | 4 |
Public Version Date | 2020-03-05 |
Device Publish Date | 2016-09-10 |
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