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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 VIROSTOP oral spray — 1 UDI-DI variant, MDR

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

Data from EUDAMED, last updated May 30, 2026

fytofontana VIROSTOP oral spray

858800394410034RU

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Herb-Pharma Corporation s.r.o.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2024-MDR/QS-023/B
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Jan 26, 2026 → Apr 18, 2029

Identity & classification

Basic UDI-DI: 858800394410034RU
Device name: fytofontana VIROSTOP oral spray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 20, 2024

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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basicUdiUlid01J0TPY32KEX55YRW9VZGK7X4M

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 VIROSTOP oral spray18588003944990