JBH

GUDID 06973175530556

Anhui JBH Medical Apparatus Co., Ltd.

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06973175530556
• NIH Device Record Key: 88ff267c-c254-4c0e-8eeb-4014b5b62fef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JBH
• Version Model Number: DC03
• 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: true
• 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	06973175530556 [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: 2025-04-08
• Device Publish Date: 2025-03-31

On-Brand Devices [JBH]

• 06973175532314: D09
• 06973175530556: DC03
• 06973175530402: D25
• 06973175530426: DC10L
• 06973175530372: D36
• 06973175530679: D16
• 06973175530419: DC07L
• 06973175530280: DC02
• 06973175530266: D26
• 06973175530228: DC03
• 06973175530204: FDB01
• 06973175530181: D15
• 06973175530167: D12
• 06973175530150: D11
• 06973175530112: D09
• 06973175530075: D05
• 06973175530044: FDB02
• 06973175530006: D10
• 06973175534059: D17
• 06973175530068: D03