FORCEMECH

GUDID 00860008903693

Foldable Electric Wheelchair

Forcemech International LLC

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

• Primary Device ID: 00860008903693
• NIH Device Record Key: 975e9989-763c-4b2d-9f99-dbef8ef65203
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FORCEMECH
• Version Model Number: NAVIGATOR XL
• Company DUNS: 098188838
• Company Name: Forcemech International LLC
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860008903693 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070501

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: 2022-10-06
• Device Publish Date: 2022-09-28

On-Brand Devices [FORCEMECH]

• 00860008903693: Foldable Electric Wheelchair
• 00860008903686: Foldable Electric Wheelchair
• 00860008903617: Foldable Electric Wheelchair
• 00860008903600: Premium Foldable Electric Wheelchair
• 00860008903624: Foldable Electric Wheelchair