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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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SURGIFIX POLIESTERE — 4 UDI-DI variants, MDR (FRA PRODUCTION SPA)

MD Atlas
FRA PRODUCTION SPA

Data from EUDAMED, last updated May 30, 2026

SURGIFIX POLIESTERE

803397155FT002GR0033K

4 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: FRA PRODUCTION SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803397155FT002GR0033K
Device name: SURGIFIX POLIESTERE
Device model: RETE TUBOLARE ELASTICA IN POLIESTERE PER TRATTENERE MEDICAZIONI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: FRA PRODUCTION SPA
SRN: IT-MF-000030441
Country: Italy
Email: info@fraproduction.it
Phone: +39 0141 979911

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01GR6PTH3NGCWYCWBBN3G1T8VR

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

0019024308033971550023
0019024508033971550047
0019024208033971550016
0019024408033971550030