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RAS-45 RRa Adult/Pediatric Acoustic Respiration Sensor

FDA UDI

Class II (US FDA UDI)

by Masimo Corporation

Identity

Trade Name
RAS-45 RRa Adult/Pediatric Acoustic Respiration Sensor FDA UDI
Generic Name
Electronic acoustic stethoscope FDA UDI
Model / Reference
4171 FDA UDI

Identifiers

Primary DI / UDI-DI
10843997009635 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Electronic acoustic stethoscope 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electronic acoustic stethoscope

RAS-45 RRa Adult/Pediatric Acoustic Respiration Sensor by Masimo Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronic acoustic stethoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Masimo Corporation

Sources (1)

  • FDA UDI 1c5e2e9b-8dca-4715-b693-dae6d3e744b6 33 fields · synced May 30, 2026