GUDID 08714729045069

Single Action Pumping System

BOSTON SCIENTIFIC CORPORATION

Urological irrigation set

• Primary Device ID: 08714729045069
• NIH Device Record Key: c6d54782-bab1-4b4f-907a-2d583c03467f
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: M0067201000
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	08714729045069 [Package]; Contains: 08714729752981; Package: [5 Units]; In Commercial Distribution
GS1	08714729752981 [Primary]

FDA Product Code

• FFY: Adaptor, bulbs, miscellaneous, for endoscope
• KQT: EVACUATOR, GASTRO-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: 2022-06-10
• Device Publish Date: 2016-09-24

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

• 08714729058632 - Contour™: 2026-02-17 Ureteral Stent Set
• 08714729058953 - Contour™: 2026-02-17 Ureteral Stent Set
• 08714729297253 - Percuflex™ Plus: 2026-02-17 Ureteral Stent Set
• 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
• 08714729424222 - Contour™: 2026-02-17 Ureteral Stent Set