AVVIGO™ Guidance System H7490097610

GUDID 08714729996538

BOSTON SCIENTIFIC CORPORATION

Cardiovascular ultrasound imaging system

• Primary Device ID: 08714729996538
• NIH Device Record Key: 52a0b8ea-d4f3-44ec-855d-0671188dbc7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AVVIGO™ Guidance System
• Version Model Number: H7490097610
• Catalog Number: H7490097610
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	08714729996538 [Primary]

FDA Product Code

• DQK: Computer, diagnostic, programmable

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: 2020-08-25
• Device Publish Date: 2020-08-17

On-Brand Devices [AVVIGO™ Guidance System]

• 08714729999966: H749009761R0
• 08714729996552: H749009761Z0
• 08714729996545: H749009761D0
• 08714729996538: H7490097610