Carlo Classic ALU Patient Lift

GUDID 04260735020605

Carlo Classic ALU Patient Lift

BEKA Hospitec GmbH

Mobile patient lifting system, electrically-powered

• Primary Device ID: 04260735020605
• NIH Device Record Key: 889ac843-99f9-430d-a158-ab57eee759ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Carlo Classic ALU Patient Lift
• Version Model Number: 924001508
• Company DUNS: 342212273
• Company Name: BEKA Hospitec GmbH
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260735020605 [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: 2025-04-08
• Device Publish Date: 2025-03-31

On-Brand Devices [Carlo Classic ALU Patient Lift]

• 04260735022425: Carlo Classic Alu Patient Lift
• 04260735022418: Carlo Classic ALU Patient Lift
• 04260735022401: Carlo Classic Alu Patient Lift
• 04260735020636: Carlo Classic ALU Patient Lift
• 04260735020629: Carlo Classic ALU Patient Lift
• 04260735020605: Carlo Classic ALU Patient Lift
• 04260735020506: Carlo Classic ALU Patient Lift
• 04260735020490: Carlo Classic ALU Patient Lift