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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Natus Keypoint — 31 UDI-DI variants, MDR (Natus Manufacturing Limited)

MD Atlas
Natus Manufacturing Limited

Data from EUDAMED, last updated May 24, 2026

Natus Keypoint

038283NA00166EN

31 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Natus Manufacturing Limited

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 038283NA00166EN
Device name: Natus Keypoint
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: Natus Manufacturing Limited
SRN: IE-MF-000000799
Country: Ireland
Email: GMB-RA.NeuralPathways@natus.com
Phone: +35391647400

Variants by status

UDI-DI variants

31 UDI-DI variants

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Applied filters

basicUdiUlid01KNSF4A9WWQZ05DXT3GBH4FA3

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

NATUS KEYPOINT G4 DESKTOP SYSTEM, GER00382830063463
NATUS KEYPOINT G4 DESKTOP SYSTEM, ITA00382830063487
NATUS KEYPOINT G4 DESKTOP UPGRADE00382830052009
Natus Stimulus Probe00382830049061
P300 Reaction Time Switch00382830048330
Single Electrical Stimulator00382830050432

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