Stretch™ VL

GUDID 08714729778103

Flexima™ Ureteral Stent Set

BOSTON SCIENTIFIC CORPORATION

Polymeric ureteral stent

• Primary Device ID: 08714729778103
• NIH Device Record Key: c674dc8e-a96b-453e-96d5-53fa811d7b3e
• Commercial Distribution Discontinuation: 2023-10-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Stretch™ VL
• Version Model Number: M006185157190
• 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: true
• 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729778103 [Primary]

FDA Product Code

• FFA: TUBE, DRAINAGE, SUPRAPUBIC

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: 2024-04-03
• Device Publish Date: 2015-09-24

On-Brand Devices [Stretch™ VL]

• 08714729789529: Flexima™ Ureteral Stent Set
• 08714729789512: Flexima™ Ureteral Stent Set
• 08714729778103: Flexima™ Ureteral Stent Set
• 08714729778097: Flexima™ Ureteral Stent Set
• 08714729777267: Flexima™ Ureteral Stent Set
• 08714729777250: Flexima™ Ureteral Stent Set
• 08714729776253: Flexima™ Ureteral Stent Set
• 08714729776284: Flexima™ Ureteral Stent Set