InterV-Curve Plus INTVMC-20-L

GUDID 15060270907944

13 Gauge 20mm Balloon Kyphoplasty Long Catheter (Micro)

PAN MEDICAL US CORPORATION

Kyphoplasty balloon catheter

• Primary Device ID: 15060270907944
• NIH Device Record Key: 30b4aa0d-28d6-4639-9dc2-2ccc0a479d8c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InterV-Curve Plus
• Version Model Number: INTVMC-20-L
• Catalog Number: INTVMC-20-L
• 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	15060270907944 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

[15060270907944]

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-Curve Plus]

• 15060270907944: 13 Gauge 20mm Balloon Kyphoplasty Long Catheter (Micro)
• 15060270907937: 13 Gauge 15mm Balloon Kyphoplasty Long Catheter (Micro)