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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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ESPARADRAPO GALENO TELA latex — 7 UDI-DI variants, MDR

MD Atlas
MARTÍNEZ LLENAS S.A.

Data from EUDAMED, last updated May 23, 2026

ESPARADRAPO GALENO TELA latex

8426059ETELAZ4

7 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: MARTÍNEZ LLENAS S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8426059ETELAZ4
Device name: ESPARADRAPO GALENO TELA latex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: MARTÍNEZ LLENAS S.A.
SRN: ES-MF-000002286
Country: Spain
Email: mllenas1@martinezllenas.com
Phone: +34 938 460 072

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9VYNQE94SGM2G4F28FP6TP

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

220113.208426059000723
435537.608426059000037
219900.208426059000747
219941.508426059000730
235581.108426059000020
235585.908426059000075
219901.908426059000754