Pegasus

GUDID 06973175531003

Anhui JBH Medical Apparatus Co., Ltd.

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06973175531003
• NIH Device Record Key: f89e7e3c-1e3c-4c6e-b125-0c13d4a53fee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pegasus
• Version Model Number: DC02
• Company DUNS: 554547530
• Company Name: Anhui JBH Medical Apparatus Co., Ltd.
• 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	06973175531003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242252

FDA Product Code

• ITI: Wheelchair, Powered

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-12
• Device Publish Date: 2025-09-04

Devices Manufactured by Anhui JBH Medical Apparatus Co., Ltd.

• 06973175530068 - JBH: 2025-09-12
• 06973175530952 - Phoenix: 2025-09-12
• 06973175530969 - Air Hawk: 2025-09-12
• 06973175530976 - Eagle HD: 2025-09-12
• 06973175531003 - Pegasus: 2025-09-12
• 06973175531003 - Pegasus: 2025-09-12
• 06973175531010 - Optimus: 2025-09-12
• 06973175531027 - Pegasus Plus HD: 2025-09-12
• 06973175531041 - Matrix Ultra 2: 2025-09-12