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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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SMARTXIDE family — 8 UDI-DI variants, MDR (DEKA M.E.L.A. SRL)

MD Atlas
DEKA M.E.L.A. SRL

Data from EUDAMED, last updated May 30, 2026

SMARTXIDE family

803410851M079XXSL

8 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: DEKA M.E.L.A. SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803410851M079XXSL
Device name: SMARTXIDE family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: DEKA M.E.L.A. SRL
SRN: IT-MF-000007389
Country: Italy
Email: info@deka.it
Phone: +39 055 8832884

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GYFK53Y7YBMPX4WZ87GPW1HN

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

M079A108034108510088
M079S108034108510484
M079C108034108510491
M079W108034108510057
M079Q208034108510040
M079BD108034108510682
M079AT108034108510422
M079BH108034108512693