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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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Non-sterile aspiration tubes — 37 UDI-DI variants, MDR

MD Atlas
Produtos Médicos Hospitalares, SA

Data from EUDAMED, last updated May 31, 2026

Non-sterile aspiration tubes

56077167038Y

37 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: Produtos Médicos Hospitalares, SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 56077167038Y
Device name: Non-sterile aspiration tubes
Device model: 703.0637
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Produtos Médicos Hospitalares, SA
SRN: PT-MF-000007631
Country: Portugal
Email: cristina.coelho@pmh.pt
Phone: +351263650680

Variants by status

UDI-DI variants

37 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ7KX8A32DWYWEJ9KVD4XXEG

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

703.400905607716040099
703.139505607716013956
703.235805607716023580
703.139305607716013932
703.062805607716006286
703.495505607716049559
703.063205607716900157
703.141005607716014106
703.0111R05607716045292
703.062705607716900140
703.157405607716015745
703.011105607716001113

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