← 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
Basic power supply, reusable FDA UDI
Device Name
Welch Allyn 767 Integrated Wall Diagnostic System including Coaxial Ophthalmoscope (#11720), MacroView Otoscope (#23810), KleenSpec Disposable Specula Dispenser, Wall-Mount Panel (34 x 12 in / 86.4 x 30.5 cm) FDA UDI
Model / Reference
901027 FDA UDI
Description
Welch Allyn 767 Integrated Wall Diagnostic System including Coaxial Ophthalmoscope (#11720), MacroView Otoscope (#23810), KleenSpec Disposable Specula Dispenser, Wall-Mount Panel (34 x 12 in / 86.4 x 30.5 cm) FDA UDI

Identifiers

Catalog Number
76792-MNOBP FDA UDI
Primary DI / UDI-DI
00732094068498 FDA UDI
FDA Product Code
HMF FDA UDI
GMDN Term
Basic power supply, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1860 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 d77df8f2-9cc8-4b32-b0a6-3ee5b2d2d757 36 fields · synced Jun 6, 2026