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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

Pneumasox Left - Small - Long — Class I MDR by BAP Medical B.V.

MD Atlas
BAP Medical B.V.

EUDAMED last updated this device on May 13, 2026

Pneumasox Left - Small - Long

5425013005081QL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BAP Medical B.V.
UDI-DI code: 05425013005050
Reference / catalog number: 40-2002

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View device family (Basic UDI)

Manufacturer information

Organization name: BAP Medical B.V.
SRN: NL-MF-000002030
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW030
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Jul 5, 2024	Still on market

Device identification

Trade name: Pneumasox Left - Small - Long
UDI-DI code: 05425013005050
Basic UDI-DI: 5425013005081QL
Reference / catalog number: 40-2002
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: PneumaSox is a static pneumatic compression device for compression therapy, to be used on the lower leg instead of bandages. It utilises air pressure. The pressure exerted on the leg by the cuff prevents oedema formation, promotes venous return and supports lymphatic drainage.
Additional information URL: https://www.bap-medical.nl/merken/pneumasox/
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)05425013005050

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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.

M03040199ELASTIC COMPRESSION BANDAGES - 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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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.