ViperWire Advance FlexTip 7-10041-03

GUDID 10852528005718

VIPERWIRE, ADVANCE FLEXTIP PERIPHERAL, .014" DIA SPRING TIP, 335CM, 5 PACK

Cardiovascular Systems, Inc.

Peripheral vascular guidewire, manual

• Primary Device ID: 10852528005718
• NIH Device Record Key: 4c788b06-6d33-423e-8fe2-b16812dc30e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ViperWire Advance FlexTip
• Version Model Number: VPR-GW-FLEX14
• Catalog Number: 7-10041-03
• Company DUNS: 024954518
• Company Name: Cardiovascular Systems, 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com
• Phone: (877) 274-0360
• Email: customerservice@csi360.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10852528005718 [Primary]
GS1	30852528005712 [Package]; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• MCW: Catheter, Peripheral, Atherectomy

Sterilization

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

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

[10852528005718]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-12-22
• Device Publish Date: 2018-06-21

On-Brand Devices [ViperWire Advance FlexTip]

• 30852528005729: VIPERWIRE, ADVANCE FLEXTIP PERIPHERAL, .014" DIA SPRING TIP, 335CM, 5 PACK
• 10852528005718: VIPERWIRE, ADVANCE FLEXTIP PERIPHERAL, .014" DIA SPRING TIP, 335CM, 5 PACK
• 30852528005323: VIPERWIRE, ADVANCE FLEXTIP PERIPHERAL, .014" DIA SPRING TIP, 335CM, 5 PACK
• 30852528005316: VIPERWIRE, ADVANCE FLEXTIP PERIPHERAL, .014" DIA SPRING TIP, 335CM, 5 PACK