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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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P8 — 2 UDI-DI variants, MDR (Medical Data Technology)

MD Atlas
Medical Data Technology

Data from EUDAMED, last updated May 23, 2026

P8

54040360P85W

2 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: Medical Data Technology

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 54040360P85W
Device name: P8
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medical Data Technology
SRN: BE-MF-000000788
Country: Belgium
Email: contact@medatec.be
Phone: 025271693

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JY4DMWZJ68ST9H12ZK4QZHR9

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

P8 - P8 rev200905404036000068
P8 - B4 rev0.405404036000075