Suction Bag 1.5l

GUDID 07612367031707

Disposable Suction Bag 1.5l for disposable collection system

Medela AG

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• Primary Device ID: 07612367031707
• NIH Device Record Key: 763c46c2-3f8b-4453-b96c-f9f2d61aaaa1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Suction Bag 1.5l
• Version Model Number: 077.0083
• Company DUNS: 488293218
• Company Name: Medela AG
• Device Count: 40
• 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: true
• Lot Batch: true
• Serial Number: false
• 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: +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	07612367013789 [Unit of Use]
GS1	07612367031325 [Primary]
GS1	07612367031707 [Package]; Contains: 07612367031325; Package: [3 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130123

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: 2016-12-20

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