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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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PANNORAMIC 250 Flash III DX Digital… — 5 UDI-DI variants, IVDR

MD Atlas
3DHISTECH Kft.

Data from EUDAMED, last updated May 24, 2026

PANNORAMIC 250 Flash III DX Digital Scanner

5999571470266JC

5 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: 3DHISTECH Kft.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 5999571470266JC
Device name: PANNORAMIC 250 Flash III DX Digital Scanner
Device model: PANNORAMIC 250 Flash III DX Digital Scanner
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: 3DHISTECH Kft.
SRN: HU-MF-000014337
Country: Hungary
Email: info@3dhistech.com
Phone: +36 1 467 5600

Variants by status

UDI-DI variants

5 UDI-DI variants

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basicUdiUlid01GPNSE1CPXHF9A8Z0RVS42096

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

PANNORAMIC 250 Flash III DX Digital Scanner05999571470181
PANNORAMIC 250 Flash III DX Digital Scanner05999571470174
PANNORAMIC 250 Flash III DX Digital Scanner05999571470266
PANNORAMIC 250 Flash III DX Digital Scanner05999571470167
PANNORAMIC 250 Flash III DX Digital Scanner05999571470198