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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
Centralized patient monitor FDA UDI
Device Name
Surveyor Central Additional Control - configured CPU English language and CD manual; 110V power; 16 monitoring slots (dual or 24" display required with additional CPU); No printer; Color LCD 24" monitor with high resolution FDA UDI
Model / Reference
901137 FDA UDI
Description
Surveyor Central Additional Control - configured CPU English language and CD manual; 110V power; 16 monitoring slots (dual or 24" display required with additional CPU); No printer; Color LCD 24" monitor with high resolution FDA UDI

Identifiers

Catalog Number
SCAC-AAA-CXCXX FDA UDI
Primary DI / UDI-DI
00732094308327 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
Centralized patient monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Centralized patient monitor

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

Similar devices

Also classified as Centralized patient monitor.

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 00fd1290-2a55-4186-854f-2a848995a4bc 35 fields · synced May 31, 2026