Raizer M 105040

GUDID 05714420050402

Raizer M manually operated lifting chair

Liftup A/S

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• Primary Device ID: 05714420050402
• NIH Device Record Key: 9205b3f8-b080-4ef0-a261-7330c48da0b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Raizer M
• Version Model Number: Raizer M
• Catalog Number: 105040
• Company DUNS: 308619001
• Company Name: Liftup A/S
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us
• Phone: +1 844 543 8878
• Email: info@liftup.us

Device Identifiers

Device Issuing Agency	Device ID
GS1	05714420050402 [Primary]

FDA Product Code

• FSA: Lift, Patient, Non-Ac-Powered

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: 2021-06-08
• Device Publish Date: 2021-05-31

Devices Manufactured by Liftup A/S

• 05714420032231 - FlexStep: 2021-06-11 FlexStep V2, 900, 3+1 step, outdoor
• 05714420032538 - FlexStep: 2021-06-11 FlexStep V2, 900, 6 step, outdoor
• 05714420033740 - FlexStep: 2021-06-11 FlexStep V2, 800, 4 step, outdoor
• 05714420034587 - FlexStep: 2021-06-11 FlexStep V2, 900, 4+1 step, outdoor
• 05714420036956 - FlexStep: 2021-06-11 FlexStep V2, 900, 3 step, outdoor
• 05714420039629 - FlexStep: 2021-06-11 FlexStep V2, 900, 5 step, outdoor
• 05714420041608 - FlexStep: 2021-06-11 FlexStep V2, 800, 3 step, outdoor
• 05714420042926 - FlexStep: 2021-06-11 FlexStep V2, 900, 2+2 step, outdoor