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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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Medical Camera — 6 UDI-DI variants, MDR

MD Atlas
Novocam Medical Innovations Oy

Data from EUDAMED, last updated May 23, 2026

Medical Camera

6429810664MC10000000QV

6 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: Novocam Medical Innovations Oy

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 6429810664MC10000000QV
Device name: Medical Camera
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: Novocam Medical Innovations Oy
SRN: FI-MF-000011728
Country: Finland
Email: info@futudent.com
Phone: +358 50 388 0008

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GSZ982GBPRET5WD1BYKAW1BS

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

EDUS06429810664044
MCCX06429810664020
PRCG06429810664037
PRCX06429810664013
CMPX06429810664051
SMCS06429810664006