Skippi Power Wheelchair for Children

GUDID 04032767402533

Otto Bock Mobility Solutions GmbH

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

• Primary Device ID: 04032767402533
• NIH Device Record Key: d3d715a7-22bf-4c76-88b4-1cc76ed53ba7
• Commercial Distribution Discontinuation: 2020-03-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Skippi Power Wheelchair for Children
• Version Model Number: 490E55=00000_X
• Company DUNS: 341148586
• Company Name: Otto Bock Mobility Solutions GmbH
• 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: false
• 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	04032767402533 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070318

FDA Product Code

• ITI: Wheelchair, Powered

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-09-16
• Device Publish Date: 2016-09-14

On-Brand Devices [Skippi Power Wheelchair for Children]

• 04032767402533: 490E55=00000_X
• 04032767048700: 490E55=00000_K