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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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EnDrive — 1 UDI-DI variant, MDR

MD Atlas
Advanced Technology Research (A.T.R.) S:R.L.

Data from EUDAMED, last updated May 30, 2026

EnDrive

805681427EnDriveJL

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Advanced Technology Research (A.T.R.) S:R.L.

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Device characteristics

Active device

Legacy certificates

Certificate number: 0425-MDR-030129-00
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ICIM S.P.A. (0425)
Validity: Mar 14, 2025 → Mar 13, 2030

Identity & classification

Basic UDI-DI: 805681427EnDriveJL
Device name: EnDrive
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 9, 2025

Manufacturer & authorised representative

Manufacturer

Name: Advanced Technology Research (A.T.R.) S:R.L.
SRN: IT-MF-000036666
Country: Italy
Email: info@atrdental.com
Phone: +390573535801

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JRCWRY5Q6GCBZ1T9XDN97X42

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

EnDrive08056814270100