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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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ZoomCam — 2 UDI-DI variants, MDR (KOBA Vision)

MD Atlas
KOBA Vision

Data from EUDAMED, last updated May 23, 2026

ZoomCam

PP12092ZOOMCAM125

2 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: KOBA Vision

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP12092ZOOMCAM125
Device name: ZoomCam
Device model: ZoomCam 1
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 24, 2023

Manufacturer & authorised representative

Manufacturer

Name: KOBA Vision
SRN: BE-MF-000000212
Country: Belgium
Email: info@kobavision.be
Phone: +3211517080

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GT1TB8YC21NFN9NSRHTBF3RC

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

DKZC1312092DKZC035
DKZCS1312092DKZCS095