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.

Kippbügel — 15 UDI-DI variants, MDR (HOYER GmbH)

MD Atlas
HOYER GmbH

Data from EUDAMED, last updated May 23, 2026

Kippbügel

426074102KippbuegelJX

15 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: HOYER 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: 426074102KippbuegelJX
Device name: Kippbügel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: HOYER GmbH
SRN: DE-MF-000007883
Country: Germany
Email: info@hoyer-lifter.com
Phone: +49 6033 96520

Variants by status

UDI-DI variants

15 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

basicUdiUlid01KFDGQZJXGT4BKHP03ESJAH71

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

9123704260741021597
9123604260741021580
9123504260741021573
9123804260741021603
9124104260741021634
9124004260741021627
9123904260741021610
9124204260741021641
9124304260741021658
7156304260741020545
9224004260741022372
7159504260741024178
9223904260741022389
7159404260741024185
7156204260741020538