VIVIDEO

GUDID 04961333242801

VIDEO PROCESSOR (FOR VIVIDEO)

PENTAX OF AMERICA, INC.

Endoscopic video image processing unit

• Primary Device ID: 04961333242801
• NIH Device Record Key: d0c856c5-d09f-44a1-9a8d-1ee0e0679df1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VIVIDEO
• Version Model Number: CP-1000
• Company DUNS: 083211284
• Company Name: PENTAX OF AMERICA, INC.
• 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: true
• Serial Number: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04961333242801 [Primary]

FDA Product Code

• PEA: Endoscope, Accessories, Image Post-Processing For Color Enhancement

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-02-21
• Device Publish Date: 2018-03-10

On-Brand Devices [VIVIDEO]

• 04961333242801: VIDEO PROCESSOR (FOR VIVIDEO)
• 04961333240067: VIDEO PROCESSOR (FOR VIVIDEO) (USED)