Manifold 125003

GUDID 06971162817246

Right on 500PSI

Tianck Medical Co., Ltd.

Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold Infusion line manifold

• Primary Device ID: 06971162817246
• NIH Device Record Key: ce6d27ab-2009-4202-9e54-345b1ac92eda
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Manifold
• Version Model Number: M-03
• Catalog Number: 125003
• 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	06971162817246 [Primary]

FDA Product Code

• DTL: Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

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 [Manifold]

• 06971162817253: Right on 500PSI
• 06971162817246: Right on 500PSI
• 06971162817239: Right on 500PSI
• 06971162812104: Right off 500PSI
• 06971162812098: Right off 500PSI
• 06971162812081: Right off 500PSI