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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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Cappetta definitiva Gekon A — 9 UDI-DI variants, MDR

MD Atlas
NEW ANCORVIS SRL

Data from EUDAMED, last updated May 30, 2026

Cappetta definitiva Gekon A

8053876-01-015NC

9 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8053876-01-015NC
Device name: Cappetta definitiva Gekon A
Device model: Cappetta definitiva Gekon A
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 2, 2023

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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HBRB8D0V0YM3GWKCMKMMPV0Y

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

CKATWMY408053876095160
CKCAMY608053876056000
CKAT08053876048043
CKATMY608053876053917
CKATLMY608053876055980
CKATLMY408053876055973
CKCAMY408053876055997
CKATPMY408053876055959
CKATPMY608053876055966