DynaRide Heavy Duty Wheelchair 22"x18" Detach Desk Arm ELR

GUDID 00616784023311

DYNAREX CORPORATION

Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible

• Primary Device ID: 00616784023311
• NIH Device Record Key: 5ce5c8f3-e649-43b5-842a-6144a715a001
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DynaRide Heavy Duty Wheelchair 22"x18" Detach Desk Arm ELR
• Version Model Number: 10233
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• 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: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616784023311 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070176

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: 2
• Public Version Date: 2019-07-22
• Device Publish Date: 2019-06-03

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