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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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Fejtámla védő — 7 UDI-DI variants, MDR (Dentalia Dentálgyártmány Kft.)

MD Atlas
Dentalia Dentálgyártmány Kft.

Data from EUDAMED, last updated May 24, 2026

Fejtámla védő

5999861682headrestcover27

7 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: Dentalia Dentálgyártmány Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5999861682headrestcover27
Device name: Fejtámla védő
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 28, 2022

Manufacturer & authorised representative

Manufacturer

Name: Dentalia Dentálgyártmány Kft.
SRN: HU-MF-000008310
Country: Hungary
Email: dentaliakft@gmail.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G8ZPNHS1J6DAVKWYG1D6ZA23

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

67002905999861682164
67002805999861682157
67000805999861682119
67000905999861682133
67000705999861682126
67002705999861682140
543605999861682171