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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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Abformlöffel, einmalige Anwendung — 37 UDI-DI variants, MDR

MD Atlas
Hager & Werken GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Abformlöffel, einmalige Anwendung

409963700020038

37 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: Hager & Werken GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 409963700020038
Device name: Abformlöffel, einmalige Anwendung
Device model: 000200
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: Hager & Werken GmbH & Co. KG
SRN: DE-MF-000004938
Country: Germany
Email: info@hagerwerken.de
Phone: +49 203 99 269 0

Variants by status

UDI-DI variants

37 UDI-DI variants

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Applied filters

basicUdiUlid01KJQDAJ5KXQ7KV4MXAQK3QHDC

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

No registered UDI-DI variants for this device family.