Acute Hemodialysis Tray 500320F

GUDID 20886333215830

Acute Hemodialysis Tray

ARGON MEDICAL DEVICES, INC.

General surgical procedure kit, medicated

• Primary Device ID: 20886333215830
• NIH Device Record Key: 98a7caae-54fd-4a9c-a950-408c650f9519
• Commercial Distribution Discontinuation: 2019-06-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Acute Hemodialysis Tray
• Version Model Number: 500320F
• Catalog Number: 500320F
• Company DUNS: 140727624
• Company Name: ARGON MEDICAL DEVICES, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333215836 [Primary]
GS1	20886333215830 [Package]; Contains: 00886333215836; Package: Box [10 Units]; Discontinued: 2019-06-03; Not in Commercial Distribution

FDA Product Code

• PPI: Hemodialysis Tray (Not A Start/Stop Kit)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-06-04
• Device Publish Date: 2016-09-23

Devices Manufactured by ARGON MEDICAL DEVICES, INC.

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• 20886333227499 - ClosureFast Guidewire: 2024-08-06 ClosureFast™ Guidewire J Tip, PTFE, Fixed Core, 0.025" (0.64mm) x 260cm
• 20886333227505 - ClosureFast Guidewire: 2024-08-06 ClosureFast™ Guidewire Double Ended, PTFE, Fixed Core 0.035" (0.89mm) x 45cm
• 20886333227512 - ClosureFast Introducer Sheath: 2024-08-06 ClosureFast Introducer Sheath Set 7Fr/Ch (2.3mm) x 7cm
• 20886333227529 - ClosureFast Introducer Sheath: 2024-08-06 ClosureFast™ Introducer Sheath Set 7Fr/Ch (2.3mm) x 11cm
• 20886333227550 - ClosureFast Micro Puncture: 2024-08-06 ClosureFast™ Micro Puncture Kit 4Fr/Ch (1.3mm)
• 20886333227567 - ClosureFast Micro Puncture: 2024-08-06 ClosureFast™ Micro Puncture Kit 5Fr/Ch (1.7mm)