Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name: Welch Allyn, Inc. FDA UDI
Generic Name: Vision physiology/eye movement analysis system FDA UDI
Device Name: VS100 UDI BASE UNIT FDA UDI
Model / Reference: 901029 FDA UDI
Description: VS100 UDI BASE UNIT FDA UDI

Identifiers

Catalog Number: VS100 FDA UDI
Primary DI / UDI-DI: 00732094214154 FDA UDI
FDA Product Code: HKO FDA UDI
GMDN Term: Vision physiology/eye movement analysis system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.1760 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Vision physiology/eye movement analysis system

Welch Allyn, Inc. by Welch Allyn, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Welch Allyn, Inc.

Sources (1)

FDA UDI 58dda380-fbdf-409e-b60a-3be19a4ebe42 35 fields · synced Jun 6, 2026