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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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CX female impression tools — 2 UDI-DI variants, MDR

MD Atlas
Hader Solutions and Distribution LTD

Data from EUDAMED, last updated May 24, 2026

CX female impression tools

5397311CXFIMPR1-23ND

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: Hader Solutions and Distribution LTD

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5397311CXFIMPR1-23ND
Device name: CX female impression tools
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: Hader Solutions and Distribution LTD
SRN: IE-MF-000014452
Country: Ireland
Email: m.herrera@hader.eu
Phone: +353870557894

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HZ7HPEA1M7YSWTDFFRAJ1H5Y

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

5011043-105397311000177
5011043-205397311000030