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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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Bandagen — 15 UDI-DI variants, MDR

MD Atlas
BODY PRODUCTS RELAX Pharma und Kosmetik GmbH

Data from EUDAMED, last updated May 23, 2026

Bandagen

42504784118MU

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: BODY PRODUCTS RELAX Pharma und Kosmetik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504784118MU
Device name: Bandagen
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: BODY PRODUCTS RELAX Pharma und Kosmetik GmbH
SRN: DE-MF-000005302
Country: Germany
Email: info@body-products.de
Phone: +49 2234 91165 0

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KFDW5Y2KR2QEW8DWD3GHJHT9

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

N640505-304250478443373
N1094104260319971286
100297-SCHU-104250478444745
N10941-304250478444721
N10941-104250478444707
N10941-404250478444738
9902104251594201779
100297-SCHU04260319971293
100297-SCHU-204250478444752
99460-104251594212270
9922204251594201168
100297-SCHU-304250478444769
N10941-204250478444714
9904904251594209195
100297-SCHU-404250478444776