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.

Inkontinenz-Auflagen — 75 UDI-DI variants, MDR

MD Atlas
BODY PRODUCTS RELAX Pharma und Kosmetik GmbH

Data from EUDAMED, last updated May 23, 2026

Inkontinenz-Auflagen

42504784509NF

75 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

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: 42504784509NF
Device name: Inkontinenz-Auflagen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 21, 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

75 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

basicUdiUlid01KFFNGE6SS2Q8X0NBY5EA9NSY

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

N15531-KUG04260444149338
73012204250478405685
730102-KUG04260444149192
N64067204250478444592
N15536-KUG04260444149161
N1236204250478411570
N64067304250478444615
N11224-caredry04250478431004
73011004250478405609
N12360-MMX04250478443717
N14994-w04250478436610
N15539-KUG04250478424549
730131-KUG04260444149291
N15534-KUG04250478424488
N1769204250478437105
N15530-KUG04260444149314
N14344-hb-ACP04250478443595
N64050704250478429926
N15528-KUG04260444149253
N12360-KUG04260444149307
N1122404250478409331
N12362-KUG04260444149178
N14995-w-ACP04250478443632
73012004250478405647
73010204250478408280

1 2 3