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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

SV-MESH-NEB-001 — Class I MDR by MIM Pharma Europe AB

MD Atlas
MIM Pharma Europe AB

EUDAMED last updated this device on Oct 14, 2025

SV-MESH-NEB-001

735017801073501780101456M

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MIM Pharma Europe AB
UDI-DI code: 07350178010145
Reference / catalog number: SV-MESH-NEB-001

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View device family (Basic UDI)

Manufacturer information

Organization name: MIM Pharma Europe AB
SRN: SE-MF-000048118
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 2 countries total.

Country	On market since	Until
SwedenPrimary placement	Nov 17, 2025	Still on market
Norway	Nov 17, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07350178010145
Basic UDI-DI: 735017801073501780101456M
Reference / catalog number: SV-MESH-NEB-001
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: Non-sterile, reusable Class I medical device intended for aerosolization of liquid medicinal or therapeutic solutions for inhalation therapy. The vibrating-mesh technology produces fine aerosol particles for efficient delivery to the upper and lower respiratory tract. Suitable for home or clinical use by adults and children under supervision. Rechargeable, portable, external use only.
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

UDI-DI DataMatrix

Encoded

(01)07350178010145

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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.

R0699NEBULISATION AND HUMIDIFICATION SYSTEMS - 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.