ThermoPro 3022

GUDID 04053815055174

Zimmer MedizinSysteme GmbH

Short-wave diathermy treatment system generator

• Primary Device ID: 04053815055174
• NIH Device Record Key: a186dc80-4885-4e97-a9a6-336f5dd0cb5c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ThermoPro
• Version Model Number: 3022
• Catalog Number: 3022
• Company DUNS: 316111251
• Company Name: Zimmer MedizinSysteme GmbH
• 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: (800) 327-3576
• Email: info@zimmerusa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04053815055174 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161862

FDA Product Code

• IMJ: Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

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: 2016-12-16

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