SKATER™ Single Step Drainage Set 756008020

GUDID 20886333000252

SKATER™ Single Step Drainage Set 8F x 20cm

ARGON MEDICAL DEVICES, INC.

Closed-wound drainage kit

• Primary Device ID: 20886333000252
• NIH Device Record Key: 6ebee7e3-90c7-4d81-bb1a-f58c920f57c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SKATER™ Single Step Drainage Set
• Version Model Number: 756008020E
• Catalog Number: 756008020
• 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

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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333000258 [Primary]
GS1	20886333000252 [Package]; Contains: 00886333000258; 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: 2022-07-20
• Device Publish Date: 2022-07-12

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

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• 20886333000276: SKATER™ Single Step Drainage Set 10Fr x 20cm
• 20886333000245: SKATER™ Single Step Drainage Set 7Fr x 25cm
• 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