MAMBA™ Flex H7493928713540

GUDID 08714729940289

Microcatheter

BOSTON SCIENTIFIC CORPORATION

Vascular microcatheter

• Primary Device ID: 08714729940289
• NIH Device Record Key: d1adadc5-a626-4617-a099-592d6691c4be
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAMBA™ Flex
• Version Model Number: H7493928713540
• Catalog Number: H7493928713540
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	08714729940289 [Primary]

FDA Product Code

• DQY: CATHETER, PERCUTANEOUS

Sterilization

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

[08714729940289]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-05-10
• Device Publish Date: 2017-11-18

On-Brand Devices [MAMBA™ Flex]

• 08714729940326: Microcatheter
• 08714729940289: Microcatheter