Sonicator Plus 992, 2 channel ME 992

GUDID 00816864020241

Microprocessor-controlled with 2 channel combination unit

METTLER ELECTRONICS CORP.

Physical therapy ultrasound/neuromuscular stimulation system

• Primary Device ID: 00816864020241
• NIH Device Record Key: b3bbfd63-a3be-41d0-a5fc-747e8d4a5469
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sonicator Plus 992, 2 channel
• Version Model Number: ME 992
• Catalog Number: ME 992
• Company DUNS: 008513913
• Company Name: METTLER ELECTRONICS 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(714)533-2221
• Email: service@mettlerelectronics.com
• Phone: +1(714)533-2221
• Email: service@mettlerelectronics.com
• Phone: +1(714)533-2221
• Email: service@mettlerelectronics.com

Device Dimensions

• Weight: 10.7 Pound
• Weight: 10.7 Pound
• Weight: 10.7 Pound

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Operating Temperture: 50-104 F
• Special Storage Condition, Specify: Between 0 and 0 *Operating Temperture: 50-104 F

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816864020241 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K984142

FDA Product Code

• LIH: INTERFERENTIAL CURRENT THERAPY

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: 2018-07-06
• Device Publish Date: 2016-09-15

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