OverTube™ M00505560

GUDID 00191506049379

Endoscopic Access System

BOSTON SCIENTIFIC CORPORATION

Endoscopic overtube, single-use

• Primary Device ID: 00191506049379
• NIH Device Record Key: 1ee06c39-3cb2-46d1-ac28-f426ee541e97
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OverTube™
• Version Model Number: M00505560
• Catalog Number: M00505560
• 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: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00191506049379 [Primary]

FDA Product Code

• FED: endoscopic access overtube, gastroenterology-urology

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-08-05
• Device Publish Date: 2025-07-28

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

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• 08714729297352 - Percuflex™ Plus: 2026-02-17 Ureteral Stent Set
• 08714729297611 - Percuflex™ Plus: 2026-02-17 Ureteral Stent Set
• 08714729339830 - Percuflex™: 2026-02-17 Ureteral Stent Set
• 08714729424123 - Contour™: 2026-02-17 Ureteral Stent Set