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Visi-Pitch Iv

FDA UDI

Class II (US FDA UDI)

by PENTAX of America, Inc.

Identity

Trade Name
VISI-PITCH IV FDA UDI
Generic Name
Electroglottograph FDA UDI
Device Name
Visi-Pitch IV FDA UDI
Model / Reference
3950B FDA UDI
Description
Visi-Pitch IV FDA UDI

Identifiers

Primary DI / UDI-DI
04961333229963 FDA UDI
FDA Product Code
KLX FDA UDI
GMDN Term
Electroglottograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1325 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electroglottograph

Visi-Pitch Iv by PENTAX of America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroglottograph.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 922a22d0-ea8d-436f-9492-f073fb52c99c 33 fields · synced May 30, 2026