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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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Ematik Lab — 4 UDI-DI variants, MDR (PROMETHEUS S.r.l.)

MD Atlas
PROMETHEUS S.r.l.

Data from EUDAMED, last updated May 31, 2026

Ematik Lab

805689325TD01HJ

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: PROMETHEUS S.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805689325TD01HJ
Device name: Ematik Lab
Device model: TD-01.01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: PROMETHEUS S.r.l.
SRN: IT-MF-000028429
Country: Italy
Email: info@ematik.it
Phone: 351 663 3305

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JVMB293P35KHN93B9FAC3MBE

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

Partisel08056893250031
PA-0108056893250024
EL-0108056893250017
EL-0108056893250000