emFieldPro 5032

GUDID 04053815074151

Zimmer MedizinSysteme GmbH

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• Primary Device ID: 04053815074151
• NIH Device Record Key: 5a29aedd-0dd6-4614-ae69-83b6e584e0af
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: emFieldPro
• Version Model Number: 5032
• Catalog Number: 5032
• 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: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com
• Phone: (888) 935-8471
• Email: coolsculpting.support@allergan.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04053815074151 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182963

FDA Product Code

• NGX: Stimulator, Muscle, Powered, For Muscle Conditioning

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: 2019-07-22
• Device Publish Date: 2019-07-12

Devices Manufactured by Zimmer MedizinSysteme GmbH

• 04053815076711 - MFG-05: 2023-10-24
• 04053815081296 - ThermoTK: 2023-06-13
• 04053815083344 - clTrac: 2023-06-13
• 04053815078562 - emField: 2022-05-19
• 04053815080848 - Cryo 7: 2022-03-09
• 24053815072915 - Zimmertrodes: 2021-03-18
• 24053815072922 - Zimmertrodes: 2021-03-18
• 24053815072939 - Zimmertrodes: 2021-03-18