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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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Divise — 5 UDI-DI variants, MDR (DEALFA S.r.l.)

MD Atlas
DEALFA S.r.l.

Data from EUDAMED, last updated May 31, 2026

Divise

805576595T0299C8

5 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: DEALFA S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805576595T0299C8
Device name: Divise
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: DEALFA S.r.l.
SRN: IT-MF-000021998
Country: Italy
Email: idefidio@dealfa.it
Phone: +390392103626

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KRXNX2B9D32KR6JMN9DYKXFE

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

NWCSM01618055765956375
NWCSM00718055765954500
NWCSM01118055765954531
NWCSM00918055765954517
NWCSM01018055765954524