InterV Flex Catheter INTVMN-20-FL

GUDID 15060270904295

11 Gauge 20mm Balloon Kyphoplasty Flex Catheter (Mini)

PAN MEDICAL US CORPORATION

Kyphoplasty balloon catheter

• Primary Device ID: 15060270904295
• NIH Device Record Key: 87685d8e-038b-4a9d-837c-23ab5b78f9eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InterV Flex Catheter
• Version Model Number: INTVMN-20-FL
• Catalog Number: INTVMN-20-FL
• Company DUNS: 080228535
• Company Name: PAN MEDICAL US CORPORATION
• 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

Customer Support Contacts

• Phone: (727) 914-3932
• Email: PanMed@PanMed.US

Device Identifiers

Device Issuing Agency	Device ID
GS1	15060270904295 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

[15060270904295]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-06-13
• Device Publish Date: 2019-06-05

On-Brand Devices [InterV Flex Catheter]

• 15060270904295: 11 Gauge 20mm Balloon Kyphoplasty Flex Catheter (Mini)
• 15056033811252: 11 Gauge 15mm Balloon Kyphoplasty Flex Catheter (Mini)