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Rd Set 4055

by Masimo Corporation

Ref 4055

Rd Set 4055 is a device classified as Class IIb in the EU and Class II in the US made by Masimo Corporation, registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 084399700000Z1T1B01V004F5), cleared under FDA 510(k) K160940 on 23 Nov 2016 and listed in FDA GUDID since 3 Jul 2020 (UDI-DI 00843997013086), active as of 24 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K160940

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084399700000Z1T1B01V004F5 Basic UDI-DI 00843997013086UDI-DIDate15 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00843997013086 UDI-DI Date3 Jul 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK160940 Date23 Nov 2016DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 084399700000Z1T1B01V004F5 registered 15 Jul 2026 Active
  • FDA 510(k) K160940 decided 23 Nov 2016 Active
  • FDA GUDID UDI-DI 00843997013086 listed 3 Jul 2020 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K160940
  2. Listed FDA GUDID 00843997013086
  3. Registered EUDAMED 084399700000Z1T1B01V004F5

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Rd Set Tf-I EUDAMED
Rd Set GUDID
Generic name
Pulse oximeter probe, reusable
Device name
RD SET Reusable Sensors
Model / reference
4055
Primary DI / UDI-DI
00843997013086
Basic UDI-DI
084399700000Z1T1B01V004F5
510(k) Number
FDA product code
DQA
EMDN code
C900301 Pulse oximeter sensors
GMDN term
Pulse oximeter probe, reusable
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
870.2700
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Pulse oximeter probe, reusable

Cleared under the same submission (K160940)

Similar devices in this category

Other devices filed under PULSE OXIMETER SENSORS.

Other devices from Masimo Corporation

See all devices from Masimo Corporation →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)