WallFlex™ Esophageal

GUDID 08714729765288

Stent System

BOSTON SCIENTIFIC CORPORATION

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• Primary Device ID: 08714729765288
• NIH Device Record Key: 73ee4aee-1666-48fe-b50a-db2b73bbc4d3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WallFlex™ Esophageal
• Version Model Number: M00516940
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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	08714729765288 [Primary]

FDA Product Code

• ESW: PROSTHESIS, ESOPHAGEAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-06-18
• Device Publish Date: 2015-09-24

On-Brand Devices [WallFlex™ Esophageal]

• 08714729778080: Stent System
• 08714729778073: Stent System
• 08714729778066: Stent System
• 08714729778059: Stent System
• 08714729778042: Stent System
• 08714729778035: Stent System
• 08714729765295: Stent System
• 08714729765288: Stent System
• 08714729765271: Stent System
• 08714729765264: Stent System
• 08714729765257: Stent System
• 08714729765240: Stent System