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.

Rumpfstützorthese — 930 UDI-DI variants, MDR

MD Atlas
Werkmeister GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Rumpfstützorthese

4048486231101YC

930 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: Werkmeister GmbH + Co. KG

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: 4048486231101YC
Device name: Rumpfstützorthese
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Werkmeister GmbH + Co. KG
SRN: DE-MF-000005120
Country: Germany
Email: info@werkmeister-gmbh.de
Phone: +49 (0) 5655 98 99 0

Variants by status

UDI-DI variants

930 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

basicUdiUlid01K42ZEA7PPWV68ZHH219B9N24

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

15KZZW04048486074036
15KZZW04048486073978
15KZZW04048486073992
15KZZW04048486073930
15KZZW04048486074012
15LG04048486074081
14LG04048486073732
14LG04048486073725
14LG04048486073817
15LG04048486074098
14LG04048486073800
14LG04048486073787
15LG04048486074104
14LG04048486073756
15LG04048486074067
15LG04048486074074
14LG04048486073749
15LG04048486074128
15LG04048486074043
14LG04048486073718
15LG04048486074142
15LG04048486074135
14LG04048486073770
14LG04048486073763
15LG04048486074050

1 2 3 4 5