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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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Heilmoor-Produkte — 8 UDI-DI variants, MDR (PharmaFit)

MD Atlas
PharmaFit

Data from EUDAMED, last updated May 23, 2026

Heilmoor-Produkte

426041329moorPC

8 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: PharmaFit

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426041329moorPC
Device name: Heilmoor-Produkte
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: PharmaFit
SRN: DE-MF-000046694
Country: Germany
Email: info@pharmafit.eu
Phone: +4938697471

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01K71NBKP8F3K7MHQZNJBYJS21

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

004204260413290108
004104260413290085
004404260413290092
009904260413290245
005504260413290061
009804260413290450
005204260413290283
005104260413290573