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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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Nocubi Cover — 2 UDI-DI variants, MDR (Nocubi AG)

MD Atlas
Nocubi AG

Data from EUDAMED, last updated May 23, 2026

Nocubi Cover

42700044928NOCUBINCUZ

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: Nocubi AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42700044928NOCUBINCUZ
Device name: Nocubi Cover
Device model: Cover
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 14, 2024

Manufacturer & authorised representative

Manufacturer

Name: Nocubi AG
SRN: CH-MF-000034743
Country: Switzerland
Email: contact-ch@nocubi.com
Phone: +41 71 588 06 15

Authorised representative

Name: Nocubi Deutschland GmbH
SRN: DE-AR-000033767
Country: Germany
Phone: +49712115989010

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01J580MENSK2ZTGNZF6XWNJPRP

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

07002220920 04270004492842
07001220920 04270004492859