Express® LD Iliac / Biliary H74938046740750

GUDID 08714729392217

Premounted Stent System

BOSTON SCIENTIFIC CORPORATION

Iliac artery stent, bare-metal

• Primary Device ID: 08714729392217
• NIH Device Record Key: bcd61fe1-53b6-4958-a14e-620aedb052e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Express® LD Iliac / Biliary
• Version Model Number: H74938046740750
• Catalog Number: H74938046740750
• 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	08714729392217 [Primary]

FDA Product Code

• NIO: STENT, ILIAC

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: 2021-02-05
• Device Publish Date: 2014-09-24

On-Brand Devices [Express® LD Iliac / Biliary]

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• 08714729392231: Premounted Stent System
• 08714729392217: Premounted Stent System
• 08714729392194: Premounted Stent System
• 08714729392170: Premounted Stent System
• 08714729392156: Premounted Stent System
• 08714729392132: Premounted Stent System
• 08714729392118: Premounted Stent System
• 08714729392095: Premounted Stent System
• 08714729392071: Premounted Stent System