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

13KZ04048486073336
13LG04048486073442
13LG04048486073435
13KZ04048486073343
13LG04048486073381
13LG04048486073480
4FLKZ04048486080013
4FLKZ04048486080006
4FLLG04048486080099
4FLKZ04048486079987
4FLKZ04048486080037
4FLLG04048486080174
4FLLG04048486080105
4FLKZ04048486079994
4FLKZ04048486080075
4FLKZ04048486080020
4FLKZ04048486080051
4FLLG04048486080112
4FLKZ04048486080082
4FLLG04048486080150
4FLKZ04048486080044
4GWLG04048486080389
4GWLG04048486080310
4GWKZ04048486080303
4GWLG04048486080402

5 6 7 8 9