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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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Compressas Tecido Não Tecido — 3 UDI-DI variants, MDR (HIDROFER SA)

MD Atlas
HIDROFER SA

Data from EUDAMED, last updated May 31, 2026

Compressas Tecido Não Tecido

073245601312622611X5

3 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: HIDROFER SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 073245601312622611X5
Device name: Compressas Tecido Não Tecido
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: HIDROFER SA
SRN: PT-MF-000002824
Country: Portugal
Email: hidrofer@hidrofer.com
Phone: +351252900530

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KG04TMQ7XWACPDCSTD61FHMQ

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

201 - 10x10 TNT Continente05601312622604
201-5x5 TNT Continente05601312622611
201-10X10 TNT CONT.BEBE05601312622628