Stingray™

GUDID 08714729837527

Guidewire with Hydrophilic Coating

BOSTON SCIENTIFIC CORPORATION

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 08714729837527
• NIH Device Record Key: 47e5220e-346a-4d0c-a13e-3ac869593670
• Commercial Distribution Discontinuation: 2023-05-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Stingray™
• Version Model Number: H749M3004A0
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	08714729837527 [Primary]

FDA Product Code

• DQX: WIRE, GUIDE, CATHETER

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: 2026-03-31
• Device Publish Date: 2016-09-24

On-Brand Devices [Stingray™]

• 08714729837503: Catheter
• 08714729837527: Guidewire with Hydrophilic Coating