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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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Organization name
UDI-DI code
Reference / catalog number

235582.8 — Class I MDR by MARTÍNEZ LLENAS S.A.

MD Atlas
MARTÍNEZ LLENAS S.A.

EUDAMED last updated this device on Apr 29, 2026

235582.8

8426059ETELALFZK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MARTÍNEZ LLENAS S.A.
UDI-DI code: 08426059000051
Reference / catalog number: 235582.8

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Manufacturer information

Organization name: MARTÍNEZ LLENAS S.A.
SRN: ES-MF-000002286
Manufacturer status: Active

Related devices

196198.38426059AAMPOW3On the market 199729.68426059AAGUAUQOn the market 196199.08426059AAMPOW3On the market 197480.88426059AAQUAWAOn the market 197481.5 8426059AAQUAWAOn the market

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08426059000051
Basic UDI-DI: 8426059ETELALFZK
Reference / catalog number: 235582.8
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Esparadrapo de tela
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M050101PLASTERS ON SPOOLS (ROLLS)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.