Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Selection devices — 29 UDI-DI variants, MDR

MD Atlas
Medimetál Gyógyászati Termékeket Gyártó és Forgalmazó Kft.

Data from EUDAMED, last updated May 24, 2026

Selection devices

59965960000000000000003JB

29 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: Medimetál Gyógyászati Termékeket Gyártó és Forgalmazó Kft.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59965960000000000000003JB
Device name: Selection devices
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 26, 2021

Manufacturer & authorised representative

Manufacturer

Name: Medimetál Gyógyászati Termékeket Gyártó és Forgalmazó Kft.
SRN: HU-MF-000004227
Country: Hungary
Email: medimetal@medimetal.hu
Phone: +36 36 415 577

Variants by status

UDI-DI variants

29 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01FNDZZTD4WRWY1SQB5EHPHVNA

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

Selection device for screw 0-80 mm05996596001147
Selection device for screw 0-80 mm05996596001185
Selection device for screw of distal femoral plate05996596297731
Selection device for screw of distal tibia plate05996596301674

1 2