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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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Dantec Keypoint G4 — 7 UDI-DI variants, MDR

MD Atlas
Natus Manufacturing Limited

Data from EUDAMED, last updated May 24, 2026

Dantec Keypoint G4

038283NA00155EH

7 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 038283NA00155EH
Device name: Dantec Keypoint G4
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 13, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KP475F1MF4PRRJ7Z0CXJEJ8J

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

KEYPOINT G4, ENG INCLUDING: CONTROL PANEL, USFF PC WITH KEYPOINT SW, 22” Mon., CART00382830049795
KEYPOINT G4, FRANCE00382830049733
KEYPOINT G4, GERMANY00382830049740
KEYPOINT G4, INTL. 230V00382830049726
KEYPOINT G4, ITALY00382830049771
KEYPOINT G4, NETHERLAND00382830049764
KEYPOINT G4, SPAIN00382830049757