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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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Genuine Grass® Silver Disc Electrodes… — 2 UDI-DI variants, MDR

MD Atlas
Natus Manufacturing Limited

Data from EUDAMED, last updated May 24, 2026

Genuine Grass® Silver Disc Electrodes - Reusable

0382830059138U7

2 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0382830059138U7
Device name: Genuine Grass® Silver Disc Electrodes - Reusable
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 27, 2021

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

2 UDI-DI variants

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basicUdiUlid01FK0SY0ZZ2TPK700SP8CE0CJ5

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

Genuine Grass® Silver Disc Electrodes - Reusable00382830017442
Genuine Grass® Silver Disc Electrodes - Reusable00382830017459