AV Sheath Tunneler AVST0200

GUDID 00801741090523

AV Sheath Tunneler Component, Handle

Bard Peripheral Vascular, Inc.

Vascular graft tunneller Vascular graft tunneller

• Primary Device ID: 00801741090523
• NIH Device Record Key: 12721dde-3c50-49c6-aef2-25bbd36df4e3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AV Sheath Tunneler
• Version Model Number: AVST0200
• Catalog Number: AVST0200
• Company DUNS: 135057938
• Company Name: Bard Peripheral Vascular, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741090523 [Primary]

FDA Product Code

• MZY: Graft,vascular,stainless steel tunneler

Sterilization

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

[00801741090523]

Moist Heat or Steam Sterilization

[00801741090523]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-19

On-Brand Devices [AV Sheath Tunneler]

• 00801741132155: AV Sheath Tunneler
• 00801741090530: AV Sheath Tunneler Set
• 00801741090523: AV Sheath Tunneler Component, Handle
• 00801741090516: AV Sheath Tunneler Sterilization Cassette