First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit 384177

GUDID 20886333209723

First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit 16GA(5F) x 65cm

ARGON MEDICAL DEVICES, INC.

Peripherally-inserted central venous catheter
Primary Device ID20886333209723
NIH Device Record Key7935a273-042e-49d0-87ba-5322ef8ef784
Commercial Distribution StatusIn Commercial Distribution
Brand NameFirst PICC™ S/L Peripherally Inserted Central Catheter Basic Kit
Version Model Number384177
Catalog Number384177
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 Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
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
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
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
GS100886333209729 [Primary]
GS120886333209723 [Package]
Contains: 00886333209729
Package: Box [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FOZCatheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-21

On-Brand Devices [First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit]

20886333223224First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit with Statlock® Stabilization
20886333209747First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit 26GA (1.9F) x 50cm
20886333209723First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit 16GA(5F) x 65cm
20886333209716First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit 18GA (4F) x 65cm
20886333209655First PICC™ S/L Peripherally Inserted Central Catheter Basic Kit 20GA (3F) x 65 cm

Trademark Results [First PICC]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FIRST PICC
FIRST PICC
74637602 2084417 Live/Registered
ARGON MEDICAL DEVICES, INC.
1995-02-23

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