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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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Aspiration tubes and drainage systems — 63 UDI-DI variants, MDR

MD Atlas
Produtos Médicos Hospitalares, SA

Data from EUDAMED, last updated May 31, 2026

Aspiration tubes and drainage systems

56077167008S

63 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: 56077167008S
Device name: Aspiration tubes and drainage systems
Device model: 703.0613
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

63 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ7K9E546HN7HT41J58YD00R

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

703.179905607716017992
705.482405607716048248
703.445805607716044585
703.062305607716006231
AMT044605607716104463
705.088405607716008846
703.063405607716006347
703.487405607716048743
701.084805607716008488
701.082105607716008211
703.486905607716048699
703.062105607716900164
701.285405607716028547

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