JBH

GUDID 06973175532314

Anhui JBH Medical Apparatus Co., Ltd.

Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible Wheelchair, electric-motor-driven, attendant/occupant-controlled, powered-steering, collapsible

• Primary Device ID: 06973175532314
• NIH Device Record Key: 7797d64a-e37a-4ef1-8034-2c2f556f3032
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JBH
• Version Model Number: D09
• 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	06973175532314 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170787

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: 2023-02-15
• Device Publish Date: 2023-02-07