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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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FESI TIFON 10/20 40 gr ± 2 — 1 UDI-DI variant, MDR (PRODCONFARM SRL)

MD Atlas
PRODCONFARM SRL

Data from EUDAMED, last updated May 30, 2026

FESI TIFON 10/20 40 gr ± 2

5944759041PRODF0410206G

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: PRODCONFARM SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5944759041PRODF0410206G
Device name: FESI TIFON 10/20 40 gr ± 2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: PRODCONFARM SRL
SRN: RO-MF-000017975
Country: Romania
Email: prodconfarm@yahoo.com
Phone: +40248206136

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01HV8WFYRFRCYBEA0DYPFJ4XGJ

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

PRODF04102005944759041431