ClosureFast Micro Puncture MPK-5F

GUDID 20886333227567

ClosureFast™ Micro Puncture Kit 5Fr/Ch (1.7mm)

ARGON MEDICAL DEVICES, INC.

General surgical procedure kit, non-medicated, reusable
Primary Device ID20886333227567
NIH Device Record Keyd2fb8a60-9f14-49dd-9321-bfee67ec2014
Commercial Distribution StatusIn Commercial Distribution
Brand NameClosureFast Micro Puncture
Version Model NumberMPK-5F
Catalog NumberMPK-5F
Company DUNS140727624
Company NameARGON MEDICAL DEVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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
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

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333227563 [Primary]
GS120886333227567 [Package]
Contains: 00886333227563
Package: Box [100 Units]
In Commercial Distribution

FDA Product Code

OFLPercutaneous Sheath Introducer Kit

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-08-06
Device Publish Date2024-07-29

On-Brand Devices [ClosureFast Micro Puncture]

20886333227567ClosureFast™ Micro Puncture Kit 5Fr/Ch (1.7mm)
20886333227550ClosureFast™ Micro Puncture Kit 4Fr/Ch (1.3mm)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.