SKATER™ Single Step Drainage Set 756510020

GUDID 20886333000382

SKATER™ Single Step Drainage Set - Locking 10F x 20cm

ARGON MEDICAL DEVICES, INC.

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• Primary Device ID: 20886333000382
• NIH Device Record Key: ff1abd68-a74c-4ace-a6ab-794e249c833f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SKATER™ Single Step Drainage Set
• Version Model Number: 756510020E
• Catalog Number: 756510020
• 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: false
• 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: true
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry and away from sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333000388 [Primary]
GS1	20886333000382 [Package]; Contains: 00886333000388; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• GBQ: Catheter, Continuous Irrigation

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-07-19
• Device Publish Date: 2022-07-11

On-Brand Devices [SKATER™ Single Step Drainage Set]

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• 20886333001310: SKATER™ Single Step Drainage Set - Locking 14F x 20cm
• 20886333001303: SKATER™ Single Step Drainage Set 16F x 25cm
• 20886333001273: Skater™ Single Step Drainage Set 10Fr x 30cm
• 20886333000412: SKATER™ Single Step Drainage Set - Locking 12F x 20cm
• 20886333000252: SKATER™ Single Step Drainage Set 8F x 20cm
• 20886333000221: SKATER™ Single Step Drainage Set 6Fr x 25cm
• 20886333001266: Skater™ Single Step Drainage Set 8Fr x 30cm