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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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Zubehör — 4 UDI-DI variants, MDR (Med SSE System GmbH)

MD Atlas
Med SSE System GmbH

Data from EUDAMED, last updated May 23, 2026

Zubehör

PP19221ZB485

4 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: Med SSE System GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP19221ZB485
Device name: Zubehör
Device model: Med SSE Zubehörartikel für Inkontinenztampons
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Med SSE System GmbH
SRN: DE-MF-000008104
Country: Germany
Email: info@medsse.de
Phone: 0911 7908806

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRE1KP1D9CMFTSMQPP90EZPD

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

7401110198501547
7400110198489594
applicator big110201484543
applicator small110201483977