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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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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

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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

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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

FP003104050235002856
FP001104050235000555
FP003004050235002788
FP003704050235003808
FP001804050235000616
FP003104050235002825
FP003104050235002818
FP002904050235002733
FP002904050235002726
FP003604050235003761
FP003104050235002849
FP002904050235002696
FP003104050235002832
FP003604050235003730
FP003704050235003822
FP003004050235002764

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