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Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Otoscope, direct FDA UDI
Device Name
Welch Allyn 3.5 V Halogen HPX Otoscope Set with MacroView Otoscope with Throat Illuminator (#23820), 60-Minute C-Cell Power Handle(s), Hard Storage Case; Reusable Ear Specula (#24400-U); Nickel-Cadmium (#72300) Battery; IEC Plug Type-A FDA UDI
Model / Reference
901079 FDA UDI
Description
Welch Allyn 3.5 V Halogen HPX Otoscope Set with MacroView Otoscope with Throat Illuminator (#23820), 60-Minute C-Cell Power Handle(s), Hard Storage Case; Reusable Ear Specula (#24400-U); Nickel-Cadmium (#72300) Battery; IEC Plug Type-A FDA UDI

Identifiers

Catalog Number
25270-M FDA UDI
Primary DI / UDI-DI
00732094011494 FDA UDI
FDA Product Code
ERA FDA UDI
GMDN Term
Otoscope, direct FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4770 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Otoscope, direct

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

Similar devices

Also classified as Otoscope, direct.

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 9d749c52-d59b-4e7c-8b47-3084ad426786 35 fields · synced May 31, 2026