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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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SKIN-B — 26 UDI-DI variants, MDR (Italfarmacia srl)

MD Atlas
Italfarmacia srl

Data from EUDAMED, last updated May 30, 2026

SKIN-B

805571533ITF0018V

26 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: Italfarmacia srl

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Device characteristics

Implantable

Legacy certificates

Certificate number: CSQ0006230623
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Jun 28, 2023 → Mar 2, 2028

Certificate number: CVD0010230223
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Jun 28, 2023 → Mar 2, 2028

Identity & classification

Basic UDI-DI: 805571533ITF0018V
Device name: SKIN-B
Device model: Linea SKIN-B
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Jun 7, 2023

Manufacturer & authorised representative

Manufacturer

Name: Italfarmacia srl
SRN: IT-MF-000013116
Country: Italy
Email: d.russotti@italfarmacia.com

Variants by status

UDI-DI variants

26 UDI-DI variants

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Applied filters

basicUdiUlid01H2AYV6SSJVP91XJHNH2Y7EY7

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

No registered UDI-DI variants for this device family.