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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
Dermatoscope, optical FDA UDI
Device Name
Welch Allyn EpiScope 3.5 V Halogen HPX Skin Surface Microscope with Rechargeable 60-Minute Power Handle(s) -- C-Cell Convertible, Soft Storage Case, C-Cell Battery Converter Accessory Not Included; Nickel-Cadmium (#72300) Battery; IEC Plug Type-E/F FDA UDI
Model / Reference
901068 FDA UDI
Description
Welch Allyn EpiScope 3.5 V Halogen HPX Skin Surface Microscope with Rechargeable 60-Minute Power Handle(s) -- C-Cell Convertible, Soft Storage Case, C-Cell Battery Converter Accessory Not Included; Nickel-Cadmium (#72300) Battery; IEC Plug Type-E/F FDA UDI

Identifiers

Catalog Number
47352 FDA UDI
Primary DI / UDI-DI
00732094072785 FDA UDI
FDA Product Code
KEH FDA UDI
GMDN Term
Dermatoscope, optical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3600 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dermatoscope, optical

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

Similar devices

Also classified as Dermatoscope, optical.

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 a6bcf946-d6a5-4058-b7a9-3e9af49a6ce2 35 fields · synced Jun 1, 2026