Sonic Systems, Inc

GUDID 00817846020051

Sonic Systems, Inc.

Ultrasonic water bath

• Primary Device ID: 00817846020051
• NIH Device Record Key: 72e868fb-565f-408e-953b-369f5965629b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sonic Systems, Inc
• Version Model Number: 246C/HL
• Company DUNS: 118481233
• Company Name: Sonic Systems, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817846020051 [Primary]

FDA Product Code

• FLG: Cleaner, Ultrasonic, Medical Instrument

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: 2023-07-26
• Device Publish Date: 2023-07-18

Devices Manufactured by Sonic Systems, Inc.

• 00817846020068 - Sonic Systems: 2023-07-27
• 00817846020259 - Belimed: 2023-07-27
• 00817846020280 - Getinge: 2023-07-27
• 00817846020297 - Getinge: 2023-07-27
• 00817846020303 - Getinge: 2023-07-27
• 00817846020310 - Belimed: 2023-07-27
• 00817846020327 - Belimed: 2023-07-27
• 00817846020341 - Belimed: 2023-07-27