Medilift

GUDID 04061591000332

Ondal Medical Systems GmbH

Medical monitor/light mount

• Primary Device ID: 04061591000332
• NIH Device Record Key: 0c7a8fb5-2356-486e-9fb1-f4249e844875
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medilift
• Version Model Number: MLFA
• Company DUNS: 313485229
• Company Name: Ondal Medical Systems 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04061591000332 [Primary]

FDA Product Code

• FQO: Table, Operating-Room, 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: 2020-09-08
• Device Publish Date: 2020-08-31

On-Brand Devices [Medilift]

• 04061591000332: MLFA
• 04061591000325: MLMA