C-Flex™ Biliary

GUDID 08714729019077

Biliary Stent

BOSTON SCIENTIFIC CORPORATION

Polymeric biliary stent, non-bioabsorbable

• Primary Device ID: 08714729019077
• NIH Device Record Key: 786475b2-9fef-4e73-b221-8fe3bebf63da
• Commercial Distribution Discontinuation: 2024-03-29
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: C-Flex™ Biliary
• Version Model Number: M00532010
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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	08714729019077 [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: 2024-04-03
• Device Publish Date: 2015-09-24

On-Brand Devices [C-Flex™ Biliary]

• 08714729019121: Biliary Stent
• 08714729019114: Biliary Stent
• 08714729019107: Biliary Stent
• 08714729019091: Biliary Stent
• 08714729019084: Biliary Stent
• 08714729019077: Biliary Stent