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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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HAT500 Tubing set — 1 UDI-DI variant, MDD (MedFact Engineering GmbH)

MD Atlas
MedFact Engineering GmbH

Data from EUDAMED, last updated May 31, 2026

HAT500 Tubing set

B-14255650100737

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: MedFact Engineering GmbH

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Device characteristics

Active deviceAdministers medicine

Legacy certificates

Certificate number: D1245800019
Type: refdata.legacy.mdd-certificate-type.v
Notified body: mdc medical device certification GmbH (0483)
Validity: May 25, 2024

Certificate number: D1245800030
Type: refdata.legacy.mdd-certificate-type.v
Notified body: mdc medical device certification GmbH (0483)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-14255650100737
Device name: HAT500 Tubing set
Device model: MF0034
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: MedFact Engineering GmbH
SRN: DE-MF-000010098
Country: Germany
Email: office@medfact.eu
Phone: +49 7621 579820

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KSJ5PG53VNRBRC6XTPDZVT3E

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

HAT500 Tubing set14255650100737