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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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Kalapácsujj korrigáló — 8 UDI-DI variants, MDR (Berkemann Hungary Bt.)

MD Atlas
Berkemann Hungary Bt.

Data from EUDAMED, last updated May 24, 2026

Kalapácsujj korrigáló

4049261KBL

8 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: Berkemann Hungary Bt.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4049261KBL
Device name: Kalapácsujj korrigáló
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: Berkemann Hungary Bt.
SRN: HU-MF-000007044
Country: Hungary
Email: csenki.t@berkemann.hu
Phone: 06308260526

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01GSA5W50RG6CJZHAQH1J05B53

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

508140/002/99004049261008321
508157/002/990 04049261008093
508154/002/65104049261008291
508154/002/65204049261008307
508154/002/64204049261008284
508154/002/64104049261008277
508154/002/63204049261008253
508154/002/63104049261008215