Manifold 121003

GUDID 06971162812098

Right off 500PSI

Tianck Medical Co., Ltd.

Infusion line manifold

• Primary Device ID: 06971162812098
• NIH Device Record Key: 5c2ed873-f9b9-4423-8491-0081073f757e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Manifold
• Version Model Number: M-03
• Catalog Number: 121003
• 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	06971162812098 [Primary]
GS1	16971162812095 [Package]; Package: middle pacage [25 Units]; In Commercial Distribution
GS1	26971162812092 [Package]; Contains: 16971162812095; Package: outer package [4 Units]; In Commercial Distribution

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