VIVIDEO

GUDID 04961333255191

VIVIDEO VIDEO PROCESSOR CP-1000 (ORDER CODE: 91035)

HOYA CORPORATION

Endoscopic video image processing unit

• Primary Device ID: 04961333255191
• NIH Device Record Key: 9aeba8ba-4f5d-410d-8565-85f002bb140b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VIVIDEO
• Version Model Number: CP-1000
• Company DUNS: 691519705
• Company Name: HOYA CORPORATION
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04961333255191 [Direct Marking]
GS1	04961333255238 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171011

FDA Product Code

• EOB: Nasopharyngoscope (Flexible Or Rigid)

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: 2025-12-29
• Device Publish Date: 2025-12-19

On-Brand Devices [VIVIDEO]

• 04961333221103: CP-1000
• 04961333255245: VIDEO NASO-PHARYNGO-LARYNGOSCOPE VNL9-CP (ORDER CODE: 91042)
• 04961333255191: VIVIDEO VIDEO PROCESSOR CP-1000 (ORDER CODE: 91035)