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.

HettCube — 12 UDI-DI variants, IVDR (Andreas Hettich GmbH)

MD Atlas
Andreas Hettich GmbH

Data from EUDAMED, last updated May 31, 2026

HettCube

04050674090001CA

12 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Andreas Hettich GmbH

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: 04050674090001CA
Device name: HettCube
Device model: 62000, 62005, 64000, 64005, 66000, 66005
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Andreas Hettich GmbH
SRN: DE-MF-000010680
Country: Germany
Email: oskar.doering@hettichlab.com
Phone: +49 7461 705 1274

Variants by status

UDI-DI variants

12 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

basicUdiUlid01KSQCXTQ1PNSRMCG35S9TD68M

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

62000-0104050674072731
6200004050674070928
62005-0104050674091183
6200504050674070911
64000-0104050674074254
6400004050674070935
64005-0104050674072748
6400504050674070904
66000-0104050674074261
6600004050674070942
66005-0104050674072878
6600504050674070898