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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® Institution — 2 UDI-DI variants, MDR (Henrotek A/S)

MD Atlas
Henrotek A/S

Data from EUDAMED, last updated May 31, 2026

HenroCup® Institution

57048312BW

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: Henrotek A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57048312BW
Device name: HenroCup® Institution
Device model: Technical aid for disabled
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01HXC2C4CPBSYYQWH8DREY6R3F

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® Institution05704831128852
HenroCup® Institution with ml.05704831128845