RAVE SL600DC

GUDID 00817650022579

Pinnacle RAVE Keyed

HARMAR SUMMIT, LLC

Stairlift, chair

• Primary Device ID: 00817650022579
• NIH Device Record Key: 7dbb9816-4f6d-4bab-b25d-75143103892d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAVE
• Version Model Number: SL600
• Catalog Number: SL600DC
• 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	00817650022579 [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: 2016-09-28

On-Brand Devices [RAVE]

• 00817650022579: Pinnacle RAVE Keyed
• 00817650022562: Pinnacle RAVE Keyed Folding Rail RH
• 00817650022555: Pinnacle RAVE Keyed Folding Rail LH
• 00817650022548: Pinnacle RAVE non Keyed Folding Rail LH
• 00817650022531: Pinnacle RAVE non Keyed Folding Rail RH
• 00817650022524: Pinnacle RAVE non Keyed
• 00817650024498: Rave-II Kit No Track
• 00817650024481: Rave-II Straight
• 00817650024474: Rave-II Folding Rail Left Hand Demo
• 00817650024450: Rave-II Folding Rail Left Hand Demo
• 00817650024443: Rave-II - RH Folding Rail Without Track
• 00817650024436: Rave-II - LH Folding Rail Without Track
• 00817650024429: Rave-II Folding Rail Right Hand Demo
• 00817650024412: Rave-II Folding Rail Right Hand
• 00817650024399: Rave-II Folding Rail Left Hand