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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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Premilled Ti Abutment — 139 UDI-DI variants, MDR (NEW ANCORVIS SRL)

MD Atlas
NEW ANCORVIS SRL

Data from EUDAMED, last updated May 30, 2026

Premilled Ti Abutment

8053876-01-007ND

139 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: NEW ANCORVIS SRL

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 8053876-01-007ND
Device name: Premilled Ti Abutment
Device model: Premilled Ti Abutment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 2, 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

139 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJR05CPMR06EE2EXXMG3Z2FJ

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

PRATEV4208053876000089
PRBR3508053876000157
PRBR4108053876000164
PRTLXWTT08053876088414
PRSMSH50T08053876065033
PRCE5008053876000218
PRST3408053876000591
PRTO40P08053876000676
PRNEGMT08053876036163
PRNS4108053876000447
PRCM5008053876000256
PRAB375T08053876000775
PRCE3408053876000195
PRABCS3750T08053876054242

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