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.

Fuß- und Finger-Druckschutz — 66 UDI-DI variants, MDR

MD Atlas
PS Product Services GmbH

Data from EUDAMED, last updated May 23, 2026

Fuß- und Finger-Druckschutz

4050235PS0004BG

66 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: PS Product Services 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: 4050235PS0004BG
Device name: Fuß- und Finger-Druckschutz
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 20, 2021

Manufacturer & authorised representative

Manufacturer

Name: PS Product Services GmbH
SRN: DE-MF-000005290
Country: Germany
Email: ulla.kaltenbach@product-services.de

Variants by status

UDI-DI variants

66 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

basicUdiUlid01FPAR6JE8KV8Q9F63QHXFGPSN

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

FP005404050235005260
FP003804050235003938
FP003304050235003068
FP005304050235005246
FP004404050235004676
FP004604050235004713
FP004804050235004850
FP004104050235003990
FP001104050235000562
FP001104050235000586
FP003604050235003754
FP001104050235000579
FP001104050235000548
FP003004050235002801
FP001804050235000647
FP002904050235002702
FP001804050235000609
FP003704050235003815
FP003704050235003792
FP001804050235000623
FP001804050235000630
FP003004050235002771
FP003004050235002795
FP003604050235003747
FP002904050235002719

1 2 3