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Radius-7 9664

by Masimo Corporation

Radius-7 9664 is a Class II device made by Masimo Corporation, listed in FDA GUDID since 16 Jul 2020 (UDI-DI 00843997009249), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00843997009249 UDI-DI Date16 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Radius-7
Generic name
Pulse Co-oximeter
Model / reference
9664
Primary DI / UDI-DI
00843997009249
FDA product code
DQA
GMDN term
Pulse Co-oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pulse Co-oximeter

Similar devices

Also classified as Pulse Co-oximeter.

Other devices from Masimo Corporation

See all devices from Masimo Corporation →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)