Skater™ Centesis Catheter 700305007

GUDID 20886333005790

Skater™ Centesis Catheter 5F x 7cm

ARGON MEDICAL DEVICES, INC.

Abdominal paracentesis needle, single-use

• Primary Device ID: 20886333005790
• NIH Device Record Key: b595e195-7a8b-4a5d-ac77-9a294fe1b995
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Skater™ Centesis Catheter
• Version Model Number: 700305007
• Catalog Number: 700305007
• 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	00886333005796 [Primary]
GS1	20886333005790 [Package]; Contains: 00886333005796; 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™ Centesis Catheter]

• 20886333005769: Skater™ Centesis Catheter 4F x 7cm
• 20886333005813: Skater™ Centesis Catheter 5F x 20cm
• 20886333005806: Skater™ Centesis Catheter 5Fr x 10cm
• 20886333005790: Skater™ Centesis Catheter 5F x 7cm
• 20886333005783: Skater™ Centesis Catheter 4Fr x 15cm
• 20886333005776: Skater™ Centesis Catheter 4Fr x 10cm
• 20886333005752: Skater™ Centesis Catheter 5F x 15cm
• 20886333005110: Skater™ Centesis Catheter 5Fr x 15cm