RUBEX AG500AC

GUDID 00817650022784

AMERIGLIDE Max OUTDOOR STAIRLIFT AC

HARMAR SUMMIT, LLC

Stairlift, chair

• Primary Device ID: 00817650022784
• NIH Device Record Key: 6510615a-0a33-4f95-b0df-7e9966b626d7
• Commercial Distribution Discontinuation: 2017-04-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RUBEX
• Version Model Number: AG500 MAX
• Catalog Number: AG500AC
• Company DUNS: 144008062
• Company Name: HARMAR SUMMIT, LLC
• 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

Customer Support Contacts

• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com
• Phone: +1(800)833-0478
• Email: quality_team@harmar.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817650022784 [Primary]

FDA Product Code

• PCD: Powered stairway chair lift

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [RUBEX]

• 00817650022784: AMERIGLIDE Max OUTDOOR STAIRLIFT AC
• 00817650022777: AMERIGLIDE OUTDOOR STAIRLIFT DC
• 00817650022760: AMERIGLIDE OUTDOOR STAIRLIFT AC
• 00817650022753: AMERIGLIDE DC STAIRLIFT
• 00817650022746: AMERIGLIDE AC STAIRLIFT
• 00817650022739: AG, ULTRA STAIRLIFT
• 00817650022685: AMERIGLIDE OUTDOOR STAIRLIFT DC
• 00817650022678: AMERIGLIDE OUTDOOR STAIRLIFT AC