Cable, Maestro 4000™

GUDID 08714729861867

Sterile Cable

BOSTON SCIENTIFIC CORPORATION

Electrical-only medical device connection cable, reusable

• Primary Device ID: 08714729861867
• NIH Device Record Key: 4cfc07bf-c70a-4abb-a1c8-3ec55a2eab48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cable, Maestro 4000™
• Version Model Number: M0046710
• 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: false
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	08714729861867 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P150005

FDA Product Code

• OAD: catheter, percutaneous, cardiac ablation, for treatment of atrial flutter

Sterilization

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

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

[08714729861867]

Ethylene Oxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2026-02-23
• Device Publish Date: 2016-03-14

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

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