← Back to catalogue

Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Ophthalmic/otologic diagnostic set FDA UDI
Device Name
Welch Allyn CompacSet 2.5 V Folding Halogen Diagnostic Set with Ophthalmoscope, Fiber-Optic Otoscope, Integrated Ear Specula Storage, Charging Accessory, Soft Storage Case; Nickel-Cadmium (#72610) Battery; IEC Plug Type-B FDA UDI
Model / Reference
901089 FDA UDI
Description
Welch Allyn CompacSet 2.5 V Folding Halogen Diagnostic Set with Ophthalmoscope, Fiber-Optic Otoscope, Integrated Ear Specula Storage, Charging Accessory, Soft Storage Case; Nickel-Cadmium (#72610) Battery; IEC Plug Type-B FDA UDI

Identifiers

Catalog Number
92100 FDA UDI
Primary DI / UDI-DI
00732094145045 FDA UDI
FDA Product Code
ERA FDA UDI
GMDN Term
Ophthalmic/otologic diagnostic set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4770 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 1e7d8130-be98-4be8-8ed3-772380e179e5 36 fields · synced Jun 1, 2026