Welch Allyn SPO2 Sensor

FDA UDI

Class II (US FDA UDI)

by Medsource International Llc

Identity

Trade Name: Welch Allyn SPO2 Sensor FDA UDI
Generic Name: Pulse oximeter probe, reprocessed FDA UDI
Device Name: SPO2 Sensor for Welch Allyn Propaq LT FDA UDI
Model / Reference: MS-WADEC4 FDA UDI
Description: SPO2 Sensor for Welch Allyn Propaq LT FDA UDI

Identifiers

Catalog Number: Not Applicable FDA UDI
Primary DI / UDI-DI: 00816703026991 FDA UDI
510(k) Number: K082787 FDA UDI
FDA Product Code: DQA FDA UDI
DXN FDA UDI
MWI FDA UDI
GMDN Term: Pulse oximeter probe, reprocessed FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2700 FDA UDI
870.1130 FDA UDI
870.2300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Pulse oximeter probe, reprocessed

Welch Allyn SPO2 Sensor by Medsource International Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medsource International Llc

Sources (1)

FDA UDI 9901ddd8-0978-4617-b1e9-d9fbe4fce98f 35 fields · synced May 31, 2026