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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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A-TAM — 3 UDI-DI variants, MDR (Med SSE System GmbH)

MD Atlas
Med SSE System GmbH

Data from EUDAMED, last updated May 23, 2026

A-TAM

PP19221AT107

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Med SSE System GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP19221AT107
Device name: A-TAM
Device model: A-Tam Analtampon
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 8, 2022

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

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GHBM9DMNW6Z5NF9281B9YVTV

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

1636111691479454
1628111691478888
1160111691480248