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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 Gekon A — 1 UDI-DI variant, MDR (NEW ANCORVIS SRL)

MD Atlas
NEW ANCORVIS SRL

Data from EUDAMED, last updated May 30, 2026

Cappetta Gekon A

8053876-01-001MZ

1 UDI-DI variant

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: 8053876-01-001MZ
Device name: Cappetta Gekon A
Device model: Cappetta 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

1 UDI-DI variant

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Applied filters

basicUdiUlid01HBR6WGRHTQRNJYDNNG6XSW9B

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

CKAT08053876018336