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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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Młotek — 29 UDI-DI variants, MDR

MD Atlas
ChM spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

Młotek

59084472NL027MF

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: ChM spółka z ograniczoną odpowiedzialnością

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 59084472NL027MF
Device name: Młotek
Device model: Hammer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: ChM spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000002121
Country: Poland
Email: chm@chm.eu
Phone: +48 858686100

Variants by status

UDI-DI variants

29 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J9BH7C0GV3MDE50KXZ4XEBCF

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

40.6087.00005908447221062
40.0077.00005908447054745
40.0283.10005908447285842
40.0074.00005908447054684

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