P.A. Catheter 497527

GUDID 20886333214703

P.A. Catheter 6F - 2 Lumen - 110cm

ARGON MEDICAL DEVICES, INC.

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Primary Device ID20886333214703
NIH Device Record Keyd3666ab0-2b34-4e82-9810-e003ab6f0c4c
Commercial Distribution Discontinuation2017-11-02
Commercial Distribution StatusNot in Commercial Distribution
Brand NameP.A. Catheter
Version Model Number497527
Catalog Number497527
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 Latextrue
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
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Dimensions

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333214709 [Primary]
GS120886333214703 [Package]
Contains: 00886333214709
Package: Box [5 Units]
Discontinued: 2017-11-02
Not in Commercial Distribution

FDA Product Code

DQOCatheter, Intravascular, Diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-12-11
Device Publish Date2016-09-21

On-Brand Devices [P.A. Catheter]

20886333214703P.A. Catheter 6F - 2 Lumen - 110cm
20886333214680P.A. Catheter 7F - 2 Lumen - 110cm

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