Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Nocubi Topper — 3 UDI-DI variants, MDR (Nocubi AG)

MD Atlas
Nocubi AG

Data from EUDAMED, last updated May 23, 2026

Nocubi Topper

42700044928NOCUBITAVF

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: Nocubi AG

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42700044928NOCUBITAVF
Device name: Nocubi Topper
Device model: Topper
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

3 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01J57YX2WZW76R8XJGWFPM967N

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

06125220920 04270004492828
06100220920 04270004492835
06065220920 04270004492811