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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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Dermasectan — 3 UDI-DI variants, MDR (DEVINTEC SAGL)

MD Atlas
DEVINTEC SAGL

Data from EUDAMED, last updated May 23, 2026

Dermasectan

7649993626FT42303VG

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: DEVINTEC SAGL

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Legacy certificates

Certificate number: IT336677
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: BUREAU VERITAS ITALIA S.P.A. (1370)
Validity: Oct 22, 2024 → Sep 7, 2028

Identity & classification

Basic UDI-DI: 7649993626FT42303VG
Device name: Dermasectan
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: DEVINTEC SAGL
SRN: CH-MF-000020271
Country: Switzerland
Email: info@devintecpharma.com
Phone: 0041916014051

Authorised representative

Name: DEVINTEC HEALTH S.L.
SRN: ES-AR-000020256
Country: Spain

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K8AMRPT0VJAH7NH72E6STRFK

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

Dermasectan07649993626151
Dermasectan07649993626182
Dermasectan07649993626175