Secondary Line M77460033

GUDID 04250273717655

Fresenius Kabi AG

Electric infusion pump administration set, single-use

• Primary Device ID: 04250273717655
• NIH Device Record Key: 7011c926-d662-44d7-9ef3-81dc7ed8cb82
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Secondary Line
• Version Model Number: SL20 FX-ND
• Catalog Number: M77460033
• Company DUNS: 315654579
• Company Name: Fresenius Kabi AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• 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: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com
• Phone: +496621168400
• Email: heinrich.martens@fresenius-kabi.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250273717655 [Package]; Contains: 04250273738421; Package: Box [50 Units]; In Commercial Distribution
GS1	04250273738421 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121613

FDA Product Code

• FRN: Pump, Infusion

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-09
• Device Publish Date: 2022-09-01

On-Brand Devices [Secondary Line]

• 04250273717655: SL20 FX-ND
• 04250273713626: SL FX