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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
Ophthalmic/otologic diagnostic set FDA UDI
Device Name
Welch Allyn Green Series 777 Integrated Wall System for Connex® Spot Monitor (CSM) or Spot Vital Signs 4400 Device (Spot) with PanOptic Basic LED Ophthalmoscope, MacroView Basic LED Otoscope, and Ear Specula Dispenser (CSM and Spot sold separately) FDA UDI
Model / Reference
901027 FDA UDI
Description
Welch Allyn Green Series 777 Integrated Wall System for Connex® Spot Monitor (CSM) or Spot Vital Signs 4400 Device (Spot) with PanOptic Basic LED Ophthalmoscope, MacroView Basic LED Otoscope, and Ear Specula Dispenser (CSM and Spot sold separately) FDA UDI

Identifiers

Catalog Number
777-PM2WCX-US FDA UDI
Primary DI / UDI-DI
00732094347029 FDA UDI
FDA Product Code
HLI FDA UDI
GMDN Term
Ophthalmic/otologic diagnostic set 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

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: Ophthalmic/otologic diagnostic set

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

Similar devices

Also classified as Ophthalmic/otologic diagnostic set.

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 44b8b393-9397-47bd-8334-e5b125dd4798 35 fields · synced Jun 1, 2026