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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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Analogo da gesso - Analogue for plaster — 364 UDI-DI variants, MDR

MD Atlas
NEW ANCORVIS SRL

Data from EUDAMED, last updated May 30, 2026

Analogo da gesso - Analogue for plaster

8053876-01-017NG

364 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: NEW ANCORVIS SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8053876-01-017NG
Device name: Analogo da gesso - Analogue for plaster
Device model: Analogo - Analogue
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: NEW ANCORVIS SRL
SRN: IT-MF-000008879
Country: Italy
Email: qualita@newancorvis.eu
Phone: +390516463070

Variants by status

UDI-DI variants

364 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J1CF8MNM79MEP2DHYDTQYTYH

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

ANTLXNT08053876085949
ANAK35-70-IO08053876009563
ANSN4808053876009150
ANMUAEGNR08053876085888
ANPD33-IO08053876008856
AN3ILP4808053876047084
ANIDMU50-IO08053876055881
ANTO40P-IO08053876009266
ANNEIS43-IO08053876054631
ANRS35-IO08053876008955
ANOS3508053876008801
ANCE4108053876008160
ANDIN-IO08053876007736
ANRS4308053876008962