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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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Physiotape — 11 UDI-DI variants, MDR

MD Atlas
BODY PRODUCTS RELAX Pharma und Kosmetik GmbH

Data from EUDAMED, last updated May 23, 2026

Physiotape

42504784318N6

11 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: 42504784318N6
Device name: Physiotape
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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KFDVHGSRMTYGZFT0NKRX1SB7

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

9923204251594201588
9923104251594201571
N11404-304250478444868
9923004251594201564
N11404-104250478444844
N11404-404250478444875
N1140404260319971279
N11404-204250478444851
N11404-504250478444882
9923304251594201601
N11404-604250478444899