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.

Abdominal- und Thoraxbandage — 223 UDI-DI variants, MDR

MD Atlas
Werkmeister GmbH + Co. KG

Data from EUDAMED, last updated May 23, 2026

Abdominal- und Thoraxbandage

4048486051101Y8

223 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: 4048486051101Y8
Device name: Abdominal- und Thoraxbandage
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 12, 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

223 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

basicUdiUlid01K2F944YMYQGJKMQET1ZQXHZF

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

316504048486117856
326504048486126773
326504048486118013
316504048486126896
316604048486126919
316204048486117795
326604048486126797
316304048486126858
326604048486118037
326604048486118044
326504048486118020
326404048486118006
316304048486126865
326304048486117986
326604048486126803
316204048486117801
316504048486126902
326104048486117948
326304048486126759
316304048486117825
316604048486117887
316604048486126926
316404048486117849
326204048486126735
316104048486126827

3 4 5 6 7