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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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NOBATRAST® OP-SET BAUCHTUCH — 6 UDI-DI variants, MDR

MD Atlas
NOBAMED Paul Danz AG

Data from EUDAMED, last updated May 23, 2026

NOBATRAST® OP-SET BAUCHTUCH

4031815601003X

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: NOBAMED Paul Danz AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4031815601003X
Device name: NOBATRAST® OP-SET BAUCHTUCH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: NOBAMED Paul Danz AG
SRN: DE-MF-000000023
Country: Germany
Email: info@nobamed-ag.com
Phone: +49 0 2335 7609 0

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KF0PWMYEFYQFF6W6D5HX5X22

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

60421904031815604028
60154404031815601621
60354404031815603625
60624404031815606220
60854404031815668624
60355604031815603724