Dispenser DP 30

GUDID ENOU4180TVS0

Infiltration pump

Nouvag AG

General-purpose infusion pump, line-powered

• Primary Device ID: ENOU4180TVS0
• NIH Device Record Key: c6df361b-9105-40c9-8fcc-f3a395bab909
• Commercial Distribution Discontinuation: 2017-12-04
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Dispenser DP 30
• Version Model Number: 4180TVS
• Company DUNS: 480610476
• Company Name: Nouvag AG
• 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: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	ENOU4180TVS0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071588

FDA Product Code

• FRN: Pump, Infusion

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-08-20
• Device Publish Date: 2017-01-13

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