Vasc Band

GUDID 06936733770320

Lepu Medical Technology (Beijing) Co.,Ltd.

Tourniquet cuff, single-use

• Primary Device ID: 06936733770320
• NIH Device Record Key: 1036b730-5343-4c05-8a0e-7693732c7c95
• Commercial Distribution Discontinuation: 2016-10-27
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Vasc Band
• Version Model Number: 3521
• Company DUNS: 529853921
• Company Name: Lepu Medical Technology (Beijing) Co.,Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06936733770320 [Primary]
GS1	26936733770324 [Package]; Package: [10 Units]; Discontinued: 2016-10-27; Not in Commercial Distribution

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

Devices Manufactured by Lepu Medical Technology (Beijing) Co.,Ltd.

• 16936733735883 - Angioway: 2020-05-06 The inflation device is applied to inflate/deflate balloon catheters and monitor pressure within the balloon.
• 16936733735890 - Angioway: 2020-05-06 The inflation device is applied to inflate/deflate balloon catheters and monitor pressure within the balloon.
• 16936733735920 - Angioway: 2020-05-06 Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary
• 16936733735937 - Angioway: 2020-05-06 Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary
• 16936733735944 - Angioway: 2020-05-06 Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary
• 16936733735951 - Angioway: 2020-05-06 Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary
• 16936733735968 - Angioway: 2020-05-06 Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary
• 16936733735975 - Angioway: 2020-05-06 Inflation Device Kits is indicated for use in percutaneous coronary Intervention (PCI) treatment (such as percutaneous coronary