V-MEDICAL

GUDID 06970237520913

Tourniquet

Xiantao Rayxin Medical Products Co., Ltd.

Arterial tourniquet, manual, single-use

• Primary Device ID: 06970237520913
• NIH Device Record Key: ea4c85bc-96ca-4a49-a9ca-ef2762283b6a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V-MEDICAL
• Version Model Number: CRTOURNI
• Company DUNS: 527157229
• Company Name: Xiantao Rayxin Medical Products 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: 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 Dimensions

• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch
• Shaft Length: 5.7 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970237520913 [Primary]
GS1	06970237520920 [Package]; Package: [100 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: 2024-12-27
• Device Publish Date: 2024-12-19