Interson 99-7901

GUDID 00850921007127

USB ultrasound probe, small parts

INTERSON CORP

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 00850921007127
• NIH Device Record Key: 12bb29f2-1e26-49b2-a44a-f996c7dbcd86
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Interson
• Version Model Number: SP-L01
• Catalog Number: 99-7901
• Company DUNS: 079884004
• Company Name: INTERSON CORP
• 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

Customer Support Contacts

• Phone: 925-462-4948
• Email: orders@interson.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850921007127 [Primary]

FDA Product Code

• IYN: System, Imaging, Pulsed Doppler, Ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-05-23
• Device Publish Date: 2017-04-27

On-Brand Devices [Interson]

• 00850921007127: USB ultrasound probe, small parts
• 00850921007004: USB ultrasound probe, general purpose/abdominal