Vanguard V1-6120-135-01

GUDID 00851616007460

The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is indicated for percutaneous transluminal angioplasty (PTA) and capture and removal of embolic material during angioplasty, for the femoral, iliac, popliteal and profunda arteries. The System is not intended for use in the renal, cerebral, coronary or carotid vasculature.

Contego Medical, Inc.

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• Primary Device ID: 00851616007460
• NIH Device Record Key: b9199ad4-a16d-4ed5-addd-e613dc553697
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vanguard
• Version Model Number: 6120x135
• Catalog Number: V1-6120-135-01
• Company DUNS: 048268128
• Company Name: Contego Medical, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com
• Phone: +1-919-459-7250
• Email: info@contegomedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851616007460 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181529

FDA Product Code

• LIT: Catheter, Angioplasty, Peripheral, Transluminal

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-13
• Device Publish Date: 2023-09-05

On-Brand Devices [Vanguard ]

• 00851616007538: The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is ind
• 00851616007460: The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is ind
• 00851616007453: The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is ind
• 00851616007385: The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is ind
• 00851616007156: The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is ind
• 00851616007149: The Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection is ind