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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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fytofontana Aurecon drops forte — 1 UDI-DI variant, MDD

MD Atlas
Herb-Pharma Corporation s.r.o.

Data from EUDAMED, last updated May 31, 2026

fytofontana Aurecon drops forte

B-04023EN

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Herb-Pharma Corporation s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-04023EN
Device name: fytofontana Aurecon drops forte
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Herb-Pharma Corporation s.r.o.
SRN: SK-MF-000005839
Country: Slovakia
Email: home@herb-pharma.com
Phone: +421 367738281

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KS8240F73XQSRC8Q430240J3

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

fytofontana Aurecon drops forteD-04023EN