RescueNet™

GUDID 10840253107425

Retrieval Device

BOSTON SCIENTIFIC CORPORATION

Gastrointestinal/airway foreign body retrieval basket, single-use

• Primary Device ID: 10840253107425
• NIH Device Record Key: ce7e337f-ae5f-4b18-a769-186d529cf80a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RescueNet™
• Version Model Number: DGN-538
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• Device Count: 5
• 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	00840253107428 [Unit of Use]
GS1	10840253107425 [Primary]

FDA Product Code

• FDI: Snare, Flexible

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2021-04-07
• Device Publish Date: 2016-09-08

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

• 08714729861867 - Cable, Maestro 4000™: 2026-02-23 Sterile Cable
• 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