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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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ALL NEW TARGET Line Med — 27 UDI-DI variants, MDR

MD Atlas
SCHNELL Trainingsgeräte GmbH

Data from EUDAMED, last updated May 23, 2026

ALL NEW TARGET Line Med

426254921ANTLMEDK6

27 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: SCHNELL Trainingsgeräte GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426254921ANTLMEDK6
Device name: ALL NEW TARGET Line Med
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: SCHNELL Trainingsgeräte GmbH
SRN: DE-MF-000033664
Country: Germany
Email: info@schnell-training.com
Phone: +49 (0) 8252 / 88 55-0

Variants by status

UDI-DI variants

27 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKV659H03A986G1CGY8H83P2

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

Shoulder & Neckpress Med04262549210029
Tricep Dip Press Med04262549210111

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