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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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FITO WRAP — 3 UDI-DI variants, MDR (PHYTO PERFORMANCE ITALIA SRL)

MD Atlas
PHYTO PERFORMANCE ITALIA SRL

Data from EUDAMED, last updated May 31, 2026

FITO WRAP

80312550014JV

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: PHYTO PERFORMANCE ITALIA SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80312550014JV
Device name: FITO WRAP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: PHYTO PERFORMANCE ITALIA SRL
SRN: IT-MF-000008118
Country: Italy
Email: info@phytoperformance.com
Phone: +39 0499001919

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KR3PAJSG5YQENQZ8TBZFEX73

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

FITO WRAP PRE-WRAP C, 7X27,5 M - BOX08031255022600
FITO WRAP PRE-WRAP CM 7X27,5 M08031255009120
JB01/L08031255038267