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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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SOPORTE ESTERNAL TALLA XS — 4 UDI-DI variants, MDR

MD Atlas
ALGRAN MANUFACTURA SANITARIA, S.L.

Data from EUDAMED, last updated May 23, 2026

SOPORTE ESTERNAL TALLA XS

8437013SPTES4Z

4 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: ALGRAN MANUFACTURA SANITARIA, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437013SPTES4Z
Device name: SOPORTE ESTERNAL TALLA XS
Device model: Z2525XS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: ALGRAN MANUFACTURA SANITARIA, S.L.
SRN: ES-MF-000042506
Country: Spain
Email: algran.sl@gmail.com
Phone: +34 65 619 57 77

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRNC1ESQ1S4D29A5M8GQTCDA

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

Z2525L08437013599306
Z2525M08437013599313
Z2525S08437013599320
Z2525XS08437013599573