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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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Fasa tifon — 3 UDI-DI variants, MDR (Deluxe Medicrafts srl)

MD Atlas
Deluxe Medicrafts srl

Data from EUDAMED, last updated May 31, 2026

Fasa tifon

5949556868FESITIFONB120UM

3 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: Deluxe Medicrafts srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5949556868FESITIFONB120UM
Device name: Fasa tifon
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Deluxe Medicrafts srl
SRN: RO-MF-000050851
Country: Romania
Email: sales@zentrum.ro

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRZYHZCD74CF3MQWD4H9BYQ5

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

890601246225205949556868144
890601246225005949556868137
890601246225105949556868120