IMPROVACUTER® Tourniquet

GUDID 16974481839545

Guangzhou Improve Medical Instruments Co., Ltd.

Venous tourniquet, single-use

• Primary Device ID: 16974481839545
• NIH Device Record Key: 96783224-bee9-40f3-805b-891967a28b9c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMPROVACUTER® Tourniquet
• Version Model Number: For Adult
• Company DUNS: 554555378
• Company Name: Guangzhou Improve Medical Instruments 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	06974481839548 [Primary]
GS1	16974481839545 [Package]; Contains: 06974481839548; Package: [50 Units]; In Commercial Distribution
GS1	46974481839546 [Package]; Package: 10x50 [10 Units]; In Commercial Distribution

FDA Product Code

• GAX: Tourniquet, Nonpneumatic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-24
• Device Publish Date: 2025-03-14

On-Brand Devices [IMPROVACUTER® Tourniquet]

• 16974481839552: For Kid
• 16974481839545: For Adult