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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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ACRY TRAY POLV. 500 GR. — 5 UDI-DI variants, MDR

MD Atlas
DENTAL MANUFACTURING S.P.A

Data from EUDAMED, last updated May 31, 2026

ACRY TRAY POLV. 500 GR.

8056865CL01PR90PV

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: DENTAL MANUFACTURING S.P.A

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8056865CL01PR90PV
Device name: ACRY TRAY POLV. 500 GR.
Device model: 0720002
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 7, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KNM6XQ4M9C7NYZ8QTBVH9NVE

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

073000208056865073026
076000208056865076027
075000208056865075020
072000208056865072029
078000208056865078021