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.

Schutzkittel — 11 UDI-DI variants, MDR

MD Atlas
BODY PRODUCTS RELAX Pharma und Kosmetik GmbH

Data from EUDAMED, last updated May 23, 2026

Schutzkittel

42504784406N4

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

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: 42504784406N4
Device name: Schutzkittel
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

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

basicUdiUlid01KFDVW1CYPFWQ8S5JCBND8MN5

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

N11333-b04250478436719
N11333-b-XL04250478437136
N11710-dg04250478412096
N64067604250478444820
N11333-y04250478409751
N1640904250478428950
N18344-y04250478444806
N11333-y-XL04250478438034
221373104250478444950
N10191-hg04250478407917
221373004250478444936