Thopaz+ 200.5718

GUDID 07612367041027

Thoracic suction System pump 079.1000

Medela AG

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• Primary Device ID: 07612367041027
• NIH Device Record Key: 8b82372d-8a38-4f38-9ba6-1cd95075980c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thopaz+
• Version Model Number: Thopaz+
• Catalog Number: 200.5718
• Company DUNS: 488293218
• Company Name: Medela AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

Customer Support Contacts

• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com
• Phone: +1-877-735-1626
• Email: info-healthcare@medela.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07612367041027 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141553

FDA Product Code

• BTA: Pump, Portable, Aspiration (Manual Or Powered)

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: 2016-09-24

On-Brand Devices [Thopaz+]

• 07612367043304: Thoracic suction system pump 079.1003
• 07612367043298: Thoracic suction system pump 079.1002
• 07612367041027: Thoracic suction System pump 079.1000