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Radical Docking Station RDS-3 signal extraction pulse oximeter

FDA UDI

Class II (US FDA UDI)

by Masimo Corporation

Identity

Trade Name
Radical Docking Station RDS-3 signal extraction pulse oximeter FDA UDI
Generic Name
Pulse oximeter, line-powered FDA UDI
Model / Reference
9172 FDA UDI

Identifiers

Primary DI / UDI-DI
00843997006057 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter, line-powered 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

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

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: Pulse oximeter, line-powered

Radical Docking Station RDS-3 signal extraction pulse oximeter by Masimo Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Masimo Corporation

Sources (1)

  • FDA UDI d671965c-8e18-45e9-9c90-1ae36fcbbeaf 33 fields · synced Jun 8, 2026