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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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ALGINATO CROMATICO 450 GR. — 2 UDI-DI variants, MDR

MD Atlas
DENTAL MANUFACTURING S.P.A

Data from EUDAMED, last updated May 31, 2026

ALGINATO CROMATICO 450 GR.

8056865CL01PR91PX

2 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: DENTAL MANUFACTURING S.P.A

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8056865CL01PR91PX
Device name: ALGINATO CROMATICO 450 GR.
Device model: 2040003
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: DENTAL MANUFACTURING S.P.A
SRN: IT-MF-000027222
Country: Italy
Email: b.piazza@europa-mdr745.it
Phone: +39 0425 51628

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQVMRQT7E9C2XYY66C907GNW

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

204000308056865204031
206000308056865206035