WHILL

GUDID 00866917000201

WHILL, INC.

Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible

• Primary Device ID: 00866917000201
• NIH Device Record Key: befa16af-57a1-4eeb-8bb7-39c59faae76f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WHILL
• Version Model Number: Model M
• Company DUNS: 079289461
• Company Name: WHILL, 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00866917000201 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153543

FDA Product Code

• ITI: Wheelchair, 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: 2018-07-06
• Device Publish Date: 2016-10-03

Devices Manufactured by WHILL, INC.

• 04570072300026 - WHILL, Inc.: 2024-09-10 The intended use of the WHILL Model C2 powered wheelchair is to provide outdoor and indoor mobility to persons limited to a seat
• 04570072300033 - WHILL, Inc.: 2024-09-10 The intended use of the WHILL Model C2 powered wheelchair is to provide outdoor and indoor mobility to persons limited to a seat
• 04570072301832 - WHILL, Inc.: 2024-09-10 The intended use of the WHILL Model F powered wheelchair is to provide outdoor and indoor mobility to persons limited to a seate
• 00866917000201 - WHILL: 2018-07-06
• 00866917000201 - WHILL: 2018-07-06