TWISTER N/A

GUDID 00606509900140

A device designed to assist a person with a disability in the techniques of selecting the correct input device in order to operate a connected primary device.

PRIDE MOBILITY PRODUCTS CORPORATION

Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques Assistive input-control operation training device, selection techniques

• Primary Device ID: 00606509900140
• NIH Device Record Key: 26e43472-b980-462e-a9ab-c5aa4da5b35a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TWISTER
• Version Model Number: TWISTER
• Catalog Number: N/A
• Company DUNS: 041477449
• Company Name: PRIDE MOBILITY PRODUCTS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00606509900140 [Primary]

FDA Product Code

• KNO: Accessories, Wheelchair

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: 2019-09-03
• Device Publish Date: 2019-08-26

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