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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 surgery instruments, Class I. — 2 UDI-DI variants, MDR

MD Atlas
BIONIKA Medline Kft.

Data from EUDAMED, last updated May 24, 2026

Dental surgery instruments, Class I.

599322003SZ

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: BIONIKA Medline Kft.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 599322003SZ
Device name: Dental surgery instruments, Class I.
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIONIKA Medline Kft.
SRN: HU-MF-000004631
Country: Hungary
Email: info@bionika.hu
Phone: +36706706875

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KS2C98CJGP551JBZCNZHF8ZZ

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

526.621.030.12005993221303515
526.621.030.18005993221303522