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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 -… — 31 UDI-DI variants, MDR

MD Atlas
Produtos Médicos Hospitalares, SA

Data from EUDAMED, last updated May 31, 2026

Non-sterile aspiration tubes - Flexivac bags

560771670492

31 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: 560771670492
Device name: Non-sterile aspiration tubes - Flexivac bags
Device model: 704.2011
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

31 UDI-DI variants

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Applied filters

basicUdiUlid01KQ7MH253TYJRBCFA93BHMN2F

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

705.201505607716020152
705.187205607716018722
705.165105607716016513
704.210005607716022286
705.176305607716017633
704.100105607716026529

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