Sonablate Insertion Pack

GUDID 00850071153071

FOCUS SURGERY INC

Invasive ultrasound transducer cooling/coupling support kit

• Primary Device ID: 00850071153071
• NIH Device Record Key: 61079bd2-3842-4b64-b166-7d9eed6de668
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sonablate Insertion Pack
• Version Model Number: 403-02200-0014-I
• Company DUNS: 101084143
• Company Name: FOCUS SURGERY INC
• 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: true
• 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	00850071153071 [Primary]

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: 2024-12-17
• Device Publish Date: 2024-12-09

On-Brand Devices [Sonablate Insertion Pack]

• 00868108000267: A combination kit consisting 1 Water Path Kit and 1 Sonablate Probe Tip Kit
• 00868108000281: A combination kit consisting 1 Water Path Kit and 1 Sonablate Probe Tip Kit.
• 00850071153095: 403-02200-0002-I
• 00850071153071: 403-02200-0014-I
• 00850071153125: 403-02200-0002-BG