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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

MB0015 — Class I MDR by MARTÍN BALART TARRIDA

MD Atlas
MARTÍN BALART TARRIDA

EUDAMED last updated this device on May 26, 2026

MB0015

8437028213TF012G

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MARTÍN BALART TARRIDA
UDI-DI code: 08437028213150
Reference / catalog number: MB0015

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View device family (Basic UDI)

Manufacturer information

Organization name: MARTÍN BALART TARRIDA
SRN: ES-MF-000044818
Manufacturer status: Active

Related devices

MB00018437028213TF022JOn the market MB00028437028213TF022JOn the market MB00038437028213TF022JOn the market MB00048437028213TF022JOn the market MB00058437028213TF022JOn the market

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.

Critical warnings

No critical warnings reported for this device.

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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: 08437028213150
Basic UDI-DI: 8437028213TF012G
Reference / catalog number: MB0015
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M0499SPECIAL DRESSINGS - OTHER

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

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