Zippie® Series Manual Wheelchair ElZ1A

GUDID 05022408045938

Zippie TS Manual Wheelchair

SUNRISE MEDICAL (US) LLC

Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible

• Primary Device ID: 05022408045938
• NIH Device Record Key: 57fad125-e68c-45d2-9a21-3b02d754bb17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zippie® Series Manual Wheelchair
• Version Model Number: ElZ1A
• Catalog Number: ElZ1A
• Company DUNS: 962525056
• Company Name: SUNRISE MEDICAL (US) LLC
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com
• Phone: +1(800)333-4000
• Email: webmaster@sunmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05022408045938 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K973673

FDA Product Code

• IOR: WHEELCHAIR, MECHANICAL

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: 2018-07-06
• Device Publish Date: 2016-08-23

On-Brand Devices [Zippie® Series Manual Wheelchair]

• 05022408046867: Zippie IRIS Manual Wheelchair
• 05022408045938: Zippie TS Manual Wheelchair