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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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Impression transfer — 7 UDI-DI variants, MDR (NEW ANCORVIS SRL)

MD Atlas
NEW ANCORVIS SRL

Data from EUDAMED, last updated May 30, 2026

Impression transfer

8053876-01-018NJ

7 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: 8053876-01-018NJ
Device name: Impression transfer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 13, 2026

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KKMBSCAFZKBBRMP3WVSKWAK3

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

TIMUAN08053876046339
TIMUA08053876009686
TI3I08053876041617
TIMUANR08053876046353
TIMUA/C08053876009693
TIMUAEGNR08053876085642
TIMUAEG08053876046322