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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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Neopren-Bandagen — 68 UDI-DI variants, MDR (PS Product Services GmbH)

MD Atlas
PS Product Services GmbH

Data from EUDAMED, last updated May 23, 2026

Neopren-Bandagen

4050235PS0005BJ

68 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: 4050235PS0005BJ
Device name: Neopren-Bandagen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 7, 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

68 UDI-DI variants

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Applied filters

basicUdiUlid01FPACXSCPP0NFKWY373NFW7SZ

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

SP012904050235002375
SP012504050235002177
SP012904050235002368
SP012504050235002160
SP012804050235002306
SP012604050235002214
SP011304050235001002
SP011304050235001019
SP012504050235002153
SP012704050235002276
SP011604050235001118
SP011304050235000999
SP012704050235002269
SP012604050235002221
SP011204050235000975
SP011504050235001088
SP011404050235001033
SP011004050235000876

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