Extractor™ Pro DL

GUDID 08714729790662

Retrieval Balloon Catheter

BOSTON SCIENTIFIC CORPORATION

ERCP catheter, balloon, non-electrical, stone-retrieval

• Primary Device ID: 08714729790662
• NIH Device Record Key: df48bfca-07fe-47a2-862e-bdde266479a3
• Commercial Distribution Discontinuation: 2024-03-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Extractor™ Pro DL
• Version Model Number: M00547220
• 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: 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: true
• 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	08714729790662 [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: 4
• Public Version Date: 2024-03-29
• Device Publish Date: 2015-09-24

On-Brand Devices [Extractor™ Pro DL]

• 08714729790662: Retrieval Balloon Catheter
• 08714729790655: Retrieval Balloon Catheter
• 08714729790631: Retrieval Balloon Catheter