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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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COR0000040 — 1 UDI-DI variant, MDD (Dima Italia S.r.l.)

MD Atlas
Dima Italia S.r.l.

Data from EUDAMED, last updated May 30, 2026

COR0000040

B-08058647921099

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Dima Italia S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-08058647921099
Device name: COR0000040
Device model: COR0000040
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Dec 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: Dima Italia S.r.l.
SRN: IT-MF-000020327
Country: Italy
Email: tech.support@dimaitalia.com
Phone: +39 051568857

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HJ5TQEVKEPCHTR57JBWB32AW

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

COR000004008058647921099