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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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Verbände — 11 UDI-DI variants, MDR (PS Product Services GmbH)

MD Atlas
PS Product Services GmbH

Data from EUDAMED, last updated May 23, 2026

Verbände

4050235PS0008BQ

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: PS Product Services GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4050235PS0008BQ
Device name: Verbände
Device model: Verbände
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 12, 2025

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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JP5ERQ2NTYR22DGVFRYAS7MQ

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

TS007804050235004034
TS007804050235004027
TS007804050235004041
TS007804050235004010
TS007204050235003709
TS007204050235003693
WV000404050235004621
TS007204050235003716
TS007204050235003686
WV000304050235004591
WV000404050235004614