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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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HEEL PRO CUP — 3 UDI-DI variants, MDR

MD Atlas
IRR spółka z ograniczoną odpowiedzialnością

Data from EUDAMED, last updated May 30, 2026

HEEL PRO CUP

59076842HEELPROCUPFX

3 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: IRR spółka z ograniczoną odpowiedzialnością

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59076842HEELPROCUPFX
Device name: —
Device model: HEEL PRO CUP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: IRR spółka z ograniczoną odpowiedzialnością
SRN: PL-MF-000024038
Country: Poland
Email: biuro@corbby.com.pl

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KJ4SW4SPZKJN3D6Q82DRQYTP

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

1731C05907684217319
1733C05907684217333
1732C05907684217326