Cobalt

GUDID 00822383284231

Cobalt X23 Red 18" Folding Seat

Drive Devilbiss Healthcare

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

• Primary Device ID: 00822383284231
• NIH Device Record Key: 4ce87eaf-0216-41e6-b05e-e3d2aec1a7bd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cobalt
• Version Model Number: COBALTX23RD16FS
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00822383284231 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070433

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: 2016-07-01

On-Brand Devices [Cobalt]

• 00822383291857: Cobalt X23 Blue 18" Folding Seat
• 00822383291840: Cobalt Red 18" Folding Seat
• 00822383291833: Cobalt Blue 18" Folding Seat
• 00822383289168: Cobalt X16 Red 18" Folding Seat
• 00822383289151: Cobalt X16 Blue 18" Folding Seat
• 00822383289144: Cobalt X14 Red 18" Folding Seat
• 00822383288925: Cobalt X14 Blue 18" Folding Seat
• 00822383284231: Cobalt X23 Red 18" Folding Seat
• 00822383284217: Cobalt Red 18" Folding Seat