Permobil

GUDID 17330818676433

PERMOBIL, INC.

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

• Primary Device ID: 17330818676433
• NIH Device Record Key: 9947f7e0-e78a-456c-95eb-84977b580a60
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Permobil
• Version Model Number: F3
• Company DUNS: 606896405
• Company Name: PERMOBIL, INC.
• 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: 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	17330818676433 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143180

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-12

On-Brand Devices [Permobil]

• 17330818889420: C300
• 17330818786507: K450
• 17330818676433: F3
• 17330818555783: Koala
• 17330818345674: M3
• 17330818334562: M5
• 17330818252319: M1
• 17330818229844: F5
• 17330818198768: M400
• 17330818123456: C350
• 17330818123401: M300
• 17330818252316: M1
• 17330818001006: F5 VS
• 17330818000993: Explorer Mini
• 17330818002003: M Corpus VS
• 17330818001334: M300 Corpus HD