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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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Cicatridina spray — 2 UDI-DI variants, MDR (FARMA-DERMA S.r.l.)

MD Atlas
FARMA-DERMA S.r.l.

Data from EUDAMED, last updated May 30, 2026

Cicatridina spray

803259587TF05EK

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: FARMA-DERMA S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803259587TF05EK
Device name: Cicatridina spray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 4, 2023

Manufacturer & authorised representative

Manufacturer

Name: FARMA-DERMA S.r.l.
SRN: IT-MF-000020737
Country: Italy
Email: quality@farmaderma.it

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H6XRCMN8R1KYKQ0Q1BK4653E

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

200508032595871347
100508032595871330