Optiflo

GUDID 08714729145264

Hemostasis Catheter

BOSTON SCIENTIFIC CORPORATION

General-purpose endoscopic needle, single-use

• Primary Device ID: 08714729145264
• NIH Device Record Key: 58528fde-047e-472d-a90e-0a403a3c6dfc
• Commercial Distribution Discontinuation: 2024-01-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Optiflo
• Version Model Number: M00511750
• 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: 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	08714729145264 [Package]; Contains: 08714729745242; Package: [5 Units]; Discontinued: 2024-01-10; Not in Commercial Distribution
GS1	08714729745242 [Primary]

FDA Product Code

• FBK: endoscopic injection needle, gastroenterology-urology

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: 2025-07-17
• Device Publish Date: 2016-09-24

On-Brand Devices [Optiflo]

• 08714729145264: Hemostasis Catheter
• 08714729144182: Hemostasis Catheter