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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

MP M — Class I MDR by VENTUBEL, S.A.

MD Atlas
VENTUBEL, S.A.

EUDAMED last updated this device on May 26, 2026

MP M

8430487METAPULGARFK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VENTUBEL, S.A.
UDI-DI code: 08430487000026
Reference / catalog number: MP M

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View device family (Basic UDI)

Manufacturer information

Organization name: VENTUBEL, S.A.
SRN: ES-MF-000039014
Manufacturer status: Active

Related devices

CO G8430487CODERAV8On the market CO M8430487CODERAV8On the market CO P8430487CODERAV8On the market MC G8430487MCORTAZSOn the market MC M8430487MCORTAZSOn 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
No usar en heridas abiertas. Una compresión excesiva puede provocar intolerancia

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Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08430487000026
Basic UDI-DI: 8430487METAPULGARFK
Reference / catalog number: MP M
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: Sujeción de la muñeca, protección de esguinces en esa zona.
Additional information URL: https://www.ventubel.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08430487000026

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

M0304010103ELASTIC COMPRESSION BANDAGES, NON-ADHESIVE, HIGH EXTENSIBILITY (>140%)

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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