Savaria

GUDID 10688503630008

Savaria Concord Lifts Inc

Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, battery-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered Mobile patient lifting system, electrically-powered

• Primary Device ID: 10688503630008
• NIH Device Record Key: fcd3a24b-caa7-4f05-ae2a-819e6c715c18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Savaria
• Version Model Number: Omega
• Company DUNS: 245449095
• Company Name: Savaria Concord Lifts Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	10688503630008 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K960276

FDA Product Code

• ING: Elevator, Wheelchair, Portable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-09-13
• Device Publish Date: 2016-09-08

On-Brand Devices [Savaria]

• 10688503690002: Stairfriend
• 10688503670004: SL1000
• 10688503640007: Delta
• 10688503630008: Omega
• 10688503610000: Multilift
• 10688503500004: Stepsaver
• 10688503410006: Prolift
• 10688503360004: M2lift
• 10688503300000: K2
• 10688503230000: C1504
• 10688503210002: V1504
• 10688503700008: Stairfriend 23