WCF

GUDID 00822383551050

WCF Wheelchair

Drive Devilbiss Healthcare

Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible

• Primary Device ID: 00822383551050
• NIH Device Record Key: d27c55ab-de0e-4398-8b26-09296a8aefd1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WCF
• Version Model Number: KG 1600BK WCF
• Company DUNS: 867673159
• Company Name: Drive Devilbiss Healthcare
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00822383551050 [Primary]

FDA Product Code

• IOR: Wheelchair, mechanical

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: 2020-07-29
• Device Publish Date: 2020-07-21

On-Brand Devices [WCF]

• 00822383551074: WCF Wheelchair
• 00822383551067: WCF Wheelchair
• 00822383551050: WCF Wheelchair
• 00822383541754: WCF Wheelchair
• 00822383562445: Provate Label Pediatric Wheelchair