VISI-PITCH

GUDID 04961333236572

VISI-PITCH (SOFTWARE)

PENTAX OF AMERICA, INC.

Electroglottograph

• Primary Device ID: 04961333236572
• NIH Device Record Key: 24858830-ff36-46f2-989b-5ac9461426b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VISI-PITCH
• Version Model Number: 3950C
• 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	04961333236572 [Primary]

FDA Product Code

• KLX: Electroglottograph

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: 2018-03-29
• Device Publish Date: 2017-11-14

On-Brand Devices [VISI-PITCH]

• 04961333245390: v4.0 VISI-PITCH WIN10 UPGRADE
• 04961333244621: VISI-PITCH IV (JAPAN)
• 04961333236572: VISI-PITCH (SOFTWARE)
• 04961333235438: VISI-PITCH