Diamondback Coronary 72010-01

GUDID 30852528005187

Guidewire, Viperwire Adavnce Coronary Floppy, .012: dia, .014" Spring Tip, 1 Pack 325 cm

Cardiovascular Systems, Inc.

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 30852528005187
• NIH Device Record Key: f6cbb4b9-e9d9-49c5-a07c-005a6b09f170
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Diamondback Coronary
• Version Model Number: GWC-12325LG-FLP
• Catalog Number: 72010-01
• 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: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com
• Phone: 651-259-1600
• Email: customerservice@csi360.com

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	10852528005183 [Primary]
GS1	30852528005187 [Package]; Contains: 10852528005183; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• MCX: Catheter, Coronary, Atherectomy

Sterilization

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

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

[30852528005187]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-12-18
• Device Publish Date: 2014-09-15

On-Brand Devices [Diamondback Coronary]

• 30852528005705: Guidewire, Viperwire Advance Coronary Flex Tip .014: dia, .012" 1 Pack 325 cm
• 10850000491363: DIAMONDBACK CORONARY, CLASSIC CROWN, 1.25MM, 135CM SHAFT
• 10850000491356: DIAMONDBACK CORONARY, CLASSIC CROWN, 1.25MM, 135CM SHAFT
• 10850026568100: DIAMONDBACK CORONARY, CLASSIC CROWN, 1.25MM, 135CM SHAFT
• 10850026568087: DIAMONDBACK CORONARY, CLASSIC CROWN, 1.25MM, 135CM SHAFT
• 10850026568698: DIAMONDBACK CORONARY, CLASSIC CROWN, 1.25MM, 135CM SHAFT
• 10852528005442: SALINE INFUSION PUMP (SIP)
• 10852528005800: SALINE INFUSION PUMP (SIP)
• 10852528005787: CORONARY ELECTRIC, CLASSIC CROWN, 1.25MM
• 10852528005336: DIAMONDBACK 360® Coronary Orbital Atherectomy System, Micro Crown
• 30852528005187: Guidewire, Viperwire Adavnce Coronary Floppy, .012: dia, .014" Spring Tip, 1 Pack 325 cm
• 10852528005176: CORONARY ELECTRIC, CLASSIC CROWN, 1.50MM
• 10852528005169: DIAMONDBACK CORONARY, CLASSIC CROWN, 1.25MM