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Welch Allyn, Inc.

FDA UDI

Class II (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Indirect binocular ophthalmoscope FDA UDI
Device Name
Welch Allyn Binocular Indirect Ophthalmoscope with Padded Headband, Yellow Filter, Diffuser Filter, Power Cord (8 ft/2.7 m), Teaching Mirror, Scleral Depressor, Fundus Chart, Small Carrying Case; Portable Power Source (#74360); China Plug Type; Chinese Language FDA UDI
Model / Reference
901023 FDA UDI
Description
Welch Allyn Binocular Indirect Ophthalmoscope with Padded Headband, Yellow Filter, Diffuser Filter, Power Cord (8 ft/2.7 m), Teaching Mirror, Scleral Depressor, Fundus Chart, Small Carrying Case; Portable Power Source (#74360); China Plug Type; Chinese Language FDA UDI

Identifiers

Catalog Number
12500-DYC FDA UDI
Primary DI / UDI-DI
00732094018776 FDA UDI
FDA Product Code
HLI FDA UDI
GMDN Term
Indirect binocular ophthalmoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1570 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Indirect binocular ophthalmoscope

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

Similar devices

Also classified as Indirect binocular ophthalmoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI f54a040b-4ef4-439d-ad61-69dc98091bc2 35 fields · synced Jun 1, 2026