← Back to catalogue

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 Station w/ S4 Wifi telemetry mon. capabilities; EN lang & CD manual; Config. CPU w/ 110V pwr & dual color LCD 24" mon.s w/ high res; Custom number of hard wired patient mon. slots & telemetry channels; Redundant server (RAID1+0) storage 1,200 days, 110V HP LaserJet printer; VERITAS analysis algorithm w/ 12-lead ECG interp, ext arrhythmia, 12-lead ST segment mon., & hemodynamic calc (req options w/ hard wired patient mon. slots); Full disclosure & SC Interface; Protocol manager FDA UDI
Model / Reference
901137 FDA UDI
Description
Surveyor Central Station w/ S4 Wifi telemetry mon. capabilities; EN lang & CD manual; Config. CPU w/ 110V pwr & dual color LCD 24" mon.s w/ high res; Custom number of hard wired patient mon. slots & telemetry channels; Redundant server (RAID1+0) storage 1,200 days, 110V HP LaserJet printer; VERITAS analysis algorithm w/ 12-lead ECG interp, ext arrhythmia, 12-lead ST segment mon., & hemodynamic calc (req options w/ hard wired patient mon. slots); Full disclosure & SC Interface; Protocol manager FDA UDI

Identifiers

Catalog Number
SCSYS-HAE-SHFCA FDA UDI
Primary DI / UDI-DI
00732094320824 FDA UDI
FDA Product Code
DPS FDA UDI
GMDN Term
Centralized patient monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2340 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

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

Manufacturer

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 3435493d-de0e-43b8-ae65-d48e996d7f1e 35 fields · synced May 30, 2026