Radial artery closure band 191002

GUDID 06971162810988

Tianck Medical Co., Ltd.

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• Primary Device ID: 06971162810988
• NIH Device Record Key: 7aca0ac3-e6e4-47b0-974b-5a41913c90af
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Radial artery closure band
• Version Model Number: TB-02
• Catalog Number: 191002
• 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	06971162810988 [Primary]

FDA Product Code

• KCY: Tourniquet, Pneumatic

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 [Radial artery closure band]

• 06971162817451: TB-03
• 06971162810988: TB-02
• 06971162810971: TB-01
• 06936841200122: TB-03M
• 06936841200092: TB-03S