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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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Intraoral scanner — 7 UDI-DI variants, MDR (CEFLA s.c.)

MD Atlas
CEFLA s.c.

Data from EUDAMED, last updated May 30, 2026

Intraoral scanner

803383793IMINTRSC1001D2

7 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: CEFLA s.c.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803383793IMINTRSC1001D2
Device name: —
Device model: Intraoral scanner
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 28, 2022

Manufacturer & authorised representative

Manufacturer

Name: CEFLA s.c.
SRN: IT-MF-000009228
Country: Italy
Email: ceflaimola@cefla.it
Phone: +39 0 542 65 31 11

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJZDJCHWQE9NH9BGYT6E5ENJ

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

7098C00308033837937159
7098C00208033837938293
7098M00308033837937135
7098B00308033837937166
7098B00208033837938309
7098N00308033837937142
7098N00208033837938286