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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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apTeleCare — 4 UDI-DI variants, MDR (Healabs)

MD Atlas
Healabs

Data from EUDAMED, last updated May 19, 2026

apTeleCare

3770031606APTC04V8

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: Healabs

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770031606APTC04V8
Device name: apTeleCare
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: May 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: Healabs
SRN: FR-MF-000033893
Country: France
Email: contact@healabs.fr

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01H1R8437S94BPPB2RE4NHFVM7

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

apTeleCare03770031606003
e-Santélys03770031606027
MyPromantis03770031606034
TSM03770031606010