Monarch

GUDID 10688503550009

Patient Lift

Savaria Concord Lifts Inc

Mobile patient lifting system, electrically-powered

• Primary Device ID: 10688503550009
• NIH Device Record Key: 7f5a8b99-2483-4bbd-8f59-01bbc24a8709
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Monarch
• Version Model Number: M929xxx
• Company DUNS: 245449095
• Company Name: Savaria Concord Lifts Inc
• 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: true
• 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	10688503550009 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-11-23
• Device Publish Date: 2017-05-30

Devices Manufactured by Savaria Concord Lifts Inc

• 10688503000610 - M-SERIES: 2024-10-16 Patient lifter
• 10688503000603 - M-SERIES: 2024-09-06 Patient lifter
• 10688503000580 - M-SERIES: 2024-08-27 Patient lifter
• 10688503000597 - M-SERIES: 2024-08-27 Patient lifter
• 10688503000573 - M-SERIES: 2024-07-26 Patient lifter
• 10688503000566 - M-SERIES: 2024-07-05 Patient lifter
• 10688503000559 - M-SERIES: 2024-06-26 Patient lifter
• 10688503000542 - M-SERIES: 2024-05-17 Patient lifter