WALLSTENT™ BILIARY

GUDID 08714729229902

Endoscopic Biliary Endoprosthesis

BOSTON SCIENTIFIC CORPORATION

Polymer-metal biliary stent, non-bioabsorbable

• Primary Device ID: 08714729229902
• NIH Device Record Key: 107934a3-597c-448c-b101-3cf49534021d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WALLSTENT™ BILIARY
• Version Model Number: H965431200
• 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

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729229902 [Primary]

FDA Product Code

• FGE: CATHETER, BILIARY, DIAGNOSTIC

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: 2021-07-22
• Device Publish Date: 2015-09-24

On-Brand Devices [WALLSTENT™ BILIARY]

• 08714729317920: Endoscopic Biliary Endoprosthesis
• 08714729229902: Endoscopic Biliary Endoprosthesis
• 08714729229872: Endoscopic Biliary Endoprosthesis
• 08714729229858: Endoscopic Biliary Endoprosthesis
• 08714729317937: Endoscopic Biliary Endoprosthesis
• 08714729317906: Endoscopic Biliary Endoprosthesis
• 08714729204688: Endoscopic Biliary Endoprosthesis
• 08714729204671: Endoscopic Biliary Endoprosthesis
• 08714729204664: Endoscopic Biliary Endoprosthesis
• 08714729204657: Endoscopic Biliary Endoprosthesis
• 08714729204640: Endoscopic Biliary Endoprosthesis
• 08714729204633: Endoscopic Biliary Endoprosthesis