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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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Medi-7 Medikamentendosierer — 3 UDI-DI variants, MDR

MD Atlas
Hasbargen Medical GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Medi-7 Medikamentendosierer

4262508951493Z6

3 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: Hasbargen Medical GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4262508951493Z6
Device name: Medi-7 Medikamentendosierer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 23, 2024

Manufacturer & authorised representative

Manufacturer

Name: Hasbargen Medical GmbH & Co. KG
SRN: DE-MF-000045551
Country: Germany
Email: post@hasbargen.de

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JFSKZ4W7G65Y30KJCH0XYSCQ

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

1493 4101042625089502014
1493 4103042625089502496
1493 4102042625089502182