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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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HenroCup — 6 UDI-DI variants, MDR (Henrotek A/S)

MD Atlas
Henrotek A/S

Data from EUDAMED, last updated May 31, 2026

HenroCup

57048311BU

6 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: Henrotek A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57048311BU
Device name: HenroCup
Device model: Technical aid for disable people
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2024

Manufacturer & authorised representative

Manufacturer

Name: Henrotek A/S
SRN: DK-MF-000029313
Country: Denmark
Email: henrotek@henrotek.com
Phone: +45 70 70 78 85

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01HX9G11GD7RCC6WD4VCSFQXMH

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

HenroCup®05704831128999
HenroCup®05704831128784
HenroCup®05704831128890
HenroCup® Clear with ml.05704831128777
HenroCup® Lid Large Lid for straw05704831128821
HenroCup® Lid Standard Lid05704831128838