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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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Injection pressure monitoring device — 2 UDI-DI variants, MDR

MD Atlas
HMC PREMEDICAL S.P.A.

Data from EUDAMED, last updated May 31, 2026

Injection pressure monitoring device

805367629TD012BSmrtTS

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: HMC PREMEDICAL S.P.A.

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 805367629TD012BSmrtTS
Device name: Injection pressure monitoring device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: HMC PREMEDICAL S.P.A.
SRN: IT-MF-000029438
Country: Italy
Email: info@hmcgroup.it
Phone: +39053522704

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K1X7ERR2MYTCMXHE0ADWE97S

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

4894000NR-0118055162480121
4894000-0118053676296641