Turkel 566075

GUDID 20884521020617

Safety Thoracentesis Procedural Tray,8 Fr/Ch (2.7 mm) x 5"" (12.7 cm) Catheter

Cardinal Health, Inc.

ENT surgical procedure kit, medicated

• Primary Device ID: 20884521020617
• NIH Device Record Key: ebda157c-4efb-49be-9342-f6515575b303
• Commercial Distribution Discontinuation: 2025-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Turkel
• Version Model Number: 566075
• Catalog Number: 566075
• Company DUNS: 080935429
• Company Name: Cardinal Health, 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: false
• 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

Device Dimensions

• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French
• Length: 5 Inch
• Catheter Gauge: 8 French

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521020610 [Primary]
GS1	20884521020617 [Package]; Contains: 10884521020610; Package: CASE [5 Units]; Discontinued: 2025-12-31; In Commercial Distribution

FDA Product Code

• GAA: NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

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: 2025-06-09
• Device Publish Date: 2018-06-27

On-Brand Devices [Turkel]

• 20884521020594: Safety Fluid Drainage System
• 20884521020631: Paracentesis Procedure Tray with Safety Components,8 Fr/Ch x 4-3/4 inch (2.7 mm x 12.1 cm) Cathe
• 20884521020617: Safety Thoracentesis Procedural Tray,8 Fr/Ch (2.7 mm) x 5"" (12.7 cm) Catheter
• 20884521020600: Safety Thoracentesis Procedural Tray,8 Fr/Ch (2.7mm) x 3-1/2"" (8.9 cm) Catheter