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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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Dental Implant Guides — 12 UDI-DI variants, MDR (DenTi System Kft.)

MD Atlas
DenTi System Kft.

Data from EUDAMED, last updated May 24, 2026

Dental Implant Guides

599957543000000000021DE

12 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: DenTi System Kft.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 599957543000000000021DE
Device name: Dental Implant Guides
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: DenTi System Kft.
SRN: HU-MF-000006488
Country: Hungary
Email: sos@dentisystem.hu
Phone: +36 63 313 023

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KG2B0BYYBNQZBFKR5RHY8XRJ

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

GHN05999575431997
BT-MU NP05999575431874
GHR05999575432000
PP05999575431980
BT-MU RP05999575431881
8000-88805999575432017
8000-88805999575434127
BT-MU RP05999575434141
GHR05999575434110
BT-MU NP05999575434134
GHN05999575434103
PP05999575434097