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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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ADAS 3D — 4 UDI-DI variants, MDR (ADAS3D MEDICAL, S.L.)

MD Atlas
ADAS3D MEDICAL, S.L.

Data from EUDAMED, last updated May 23, 2026

ADAS 3D

8437021722ADAS3DWX

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: ADAS3D MEDICAL, S.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8437021722ADAS3DWX
Device name: ADAS 3D
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: ADAS3D MEDICAL, S.L.
SRN: ES-MF-000000391
Country: Spain
Email: info@adas3d.com
Phone: +34 93 328 39 64

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FH8K92482816M2H6C0Q0FR3Y

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

ADAS 3D ver. 2.1208437021722079
ADAS 3D ver. 2.1108437021722062
ADAS 3D ver. 2.908437021722017
ADAS 3D ver. 2.1308437021722093