Closed suction catheter 221003

GUDID 06971162811800

Tianck Medical Co., Ltd.

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• Primary Device ID: 06971162811800
• NIH Device Record Key: c761cc1e-e18f-477f-9253-bb6786168b80
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Closed suction catheter
• Version Model Number: 10F
• Catalog Number: 221003
• Company DUNS: 418642903
• Company Name: Tianck Medical Co., Ltd.
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971162811800 [Primary]

FDA Product Code

• JOL: Catheter And Tip, Suction

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: 2023-02-14
• Device Publish Date: 2023-02-06

On-Brand Devices [Closed suction catheter]

• 06971162811831: 16F
• 06971162811824: 14F
• 06971162811817: 12F
• 06971162811800: 10F
• 06971162811794: 8F
• 06971162811787: 6F