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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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reprop — 6 UDI-DI variants, MDR (Practomed UG)

MD Atlas
Practomed UG

Data from EUDAMED, last updated May 23, 2026

reprop

PP05394KG65

6 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: Practomed UG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP05394KG65
Device name: reprop
Device model: reprop
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Practomed UG
SRN: DE-MF-000013189
Country: Germany
Email: info@practomed.de
Phone: +49 7621 401240‬

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KRG2PPDFA7BKFNQ405KJEPK1

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

PR101110012371943
PR104111622380205
PR102110012373172
PR105111622381992
PR103110062430935
PR106111155061409