Vaccess® VA5052

GUDID 00801741059629

Vaccess® PTA Dilatation Catheter 5 mm x 20 mm, 50 cm Catheter

Bard Peripheral Vascular, Inc.

Peripheral angioplasty balloon catheter, basic

• Primary Device ID: 00801741059629
• NIH Device Record Key: b5c2f057-6102-4abf-a40c-e80b3d82b6bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vaccess®
• Version Model Number: VA5052
• Catalog Number: VA5052
• Company DUNS: 135057938
• Company Name: Bard Peripheral Vascular, Inc.
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741059629 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111850

FDA Product Code

• LIT: Catheter, angioplasty, peripheral, transluminal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-09
• Device Publish Date: 2016-08-08

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• 00801741059902: Vaccess® PTA Dilatation Catheter 7 mm x 20 mm, 80 cm Catheter
• 00801741059896: Vaccess® PTA Dilatation Catheter 6 mm x 80 mm, 80 cm Catheter
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• 00801741059872: Vaccess® PTA Dilatation Catheter 6 mm x 40 mm, 80 cm Catheter
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• 00801741059827: Vaccess® PTA Dilatation Catheter 4 mm x 80 mm, 80 cm Catheter
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