Hemostasis Valve 497297

GUDID 10886333214300

Hemostasis Valve 7F-9F

ARGON MEDICAL DEVICES, INC.

Haemostasis valve
Primary Device ID10886333214300
NIH Device Record Keyf1c0cf88-8593-4bbd-80cc-a72d76a9b4a7
Commercial Distribution StatusIn Commercial Distribution
Brand NameHemostasis Valve
Version Model Number497297
Catalog Number497297
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
GS100886333214303 [Primary]
GS110886333214300 [Package]
Contains: 00886333214303
Package: Box [10 Units]
In Commercial Distribution
GS120886333214307 [Package]
Contains: 00886333214303
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 Date2016-09-09

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