Hemostasis Valve 4F-6F 497296

GUDID 10886333214294

Hemostasis Valve 4F-6F

ARGON MEDICAL DEVICES, INC.

Haemostasis valve Haemostasis valve
Primary Device ID10886333214294
NIH Device Record Key8646b40f-23bc-47c2-a956-176c364ca8f9
Commercial Distribution StatusIn Commercial Distribution
Brand NameHemostasis Valve 4F-6F
Version Model Number497296
Catalog Number497296
Company DUNS140727624
Company NameARGON MEDICAL DEVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333214297 [Primary]
GS110886333214294 [Package]
Contains: 00886333214297
Package: Box [10 Units]
In Commercial Distribution
GS120886333214291 [Package]
Contains: 00886333214297
Package: Box [40 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DREDilator, Vessel, For Percutaneous Catheterization

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-03-05
Device Publish Date2016-09-10

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