SpyScope

GUDID 08714729764434

Access and Delivery Catheter

BOSTON SCIENTIFIC CORPORATION

Flexible fibreoptic gastroduodenoscope

• Primary Device ID: 08714729764434
• NIH Device Record Key: 4921f999-1cf1-4bfe-b732-5bd1452b544e
• Commercial Distribution Discontinuation: 2020-01-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: SpyScope
• Version Model Number: M00546230
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729764434 [Primary]

FDA Product Code

• ODF: Mini endoscope, 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: 2020-10-20
• Device Publish Date: 2016-09-24

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

• 00191506044466 - WallFlex™: 2025-03-11 Stent System
• 00191506044473 - WallFlex™: 2025-03-11 Stent System
• 00191506044480 - WallFlex™: 2025-03-11 Stent System
• 00191506044497 - WallFlex™: 2025-03-11 Stent System
• 00191506044503 - WallFlex™: 2025-03-11 Stent System
• 00191506044510 - WallFlex™: 2025-03-11 Stent System
• 00191506044527 - WallFlex™: 2025-03-11 Stent System
• 08714729035886 - NA: 2025-03-11 Torque Vise