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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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Recipiente muestras orina con STI (24… — 9 UDI-DI variants, IVDR

MD Atlas
ENVASES FARMACÉUTICOS, S.A.

Data from EUDAMED, last updated May 23, 2026

Recipiente muestras orina con STI (24 horas)

8431785UDI-DI-076T

9 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: ENVASES FARMACÉUTICOS, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431785UDI-DI-076T
Device name: Recipiente muestras orina con STI (24 horas)
Device model: Recipiente muestra de orina con sistema de transferencia integrado (24 horas)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jul 15, 2022

Manufacturer & authorised representative

Manufacturer

Name: ENVASES FARMACÉUTICOS, S.A.
SRN: ES-MF-000000902
Country: Spain
Email: info@enfa.es
Phone: +34 916 580 936

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01G811MXNWYW8P7N42VTCDADMC

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

72F08431785002811
72G08431785002828
72H08431785002835
72P08431785001098
72D08431785001050
72U08431785003665
72PRO08431785003672
72V08431785003658
72W08470001986016