← 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
Patient monitoring system module, electrocardiographic FDA UDI
Device Name
Nellcor OxiCliq Reuseable Cable,(for use with OXICLIQ-PI sensor) (3.0 ft/.91 m) FDA UDI
Model / Reference
901012 FDA UDI
Description
Nellcor OxiCliq Reuseable Cable,(for use with OXICLIQ-PI sensor) (3.0 ft/.91 m) FDA UDI

Identifiers

Catalog Number
OC-3 FDA UDI
Primary DI / UDI-DI
00732094075175 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Patient monitoring system module, electrocardiographic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient monitoring system module, electrocardiographic

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

Similar devices

Also classified as Patient monitoring system module, electrocardiographic.

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 d42e641f-a49f-4bd3-bc2a-e760a93fad99 35 fields · synced May 30, 2026