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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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M2 200kg — 2 UDI-DI variants, MDR (HMN A/S)

MD Atlas
HMN A/S

Data from EUDAMED, last updated May 31, 2026

M2 200kg

5707526M2_200KGJW

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: HMN A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5707526M2_200KGJW
Device name: —
Device model: M2 200kg
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 27, 2022

Manufacturer & authorised representative

Manufacturer

Name: HMN A/S
SRN: DK-MF-000002137
Country: Denmark
Email: km@hmnpolen.pl
Phone: +45 43 96 24 00

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G6WT2MC715KR4H2AB018BVCE

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

M2 200kg05707526000686
M2 200kg with netweave05707526001331