Contour™ SureDrive™

GUDID 08714729903239

Steerable Ureteral Stent Set

BOSTON SCIENTIFIC CORPORATION

Polymeric ureteral stent

• Primary Device ID: 08714729903239
• NIH Device Record Key: ef02d36d-3cee-48b5-8996-33f3003b53f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Contour™ SureDrive™
• Version Model Number: M0061458680
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729903239 [Primary]

FDA Product Code

• FAD: STENT, URETERAL

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: 2026-01-16
• Device Publish Date: 2017-11-03

On-Brand Devices [Contour™ SureDrive™]

• 08714729903277: Steerable Ureteral Stent Set
• 08714729903260: Steerable Ureteral Stent Set
• 08714729903253: Steerable Ureteral Stent Set
• 08714729903246: Steerable Ureteral Stent Set
• 08714729903239: Steerable Ureteral Stent Set
• 08714729903222: Steerable Ureteral Stent Set
• 08714729903215: Steerable Ureteral Stent Set
• 08714729903208: Steerable Ureteral Stent Set
• 08714729903192: Steerable Ureteral Stent Set
• 08714729903185: Steerable Ureteral Stent Set
• 08714729903178: Steerable Ureteral Stent Set
• 08714729903161: Steerable Ureteral Stent Set
• 08714729903154: Steerable Ureteral Stent Set
• 08714729903147: Steerable Ureteral Stent Set