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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

SinaVita® Immune Support Oral Spray — Class I MDR

MD Atlas
MIM Pharma Europe AB

EUDAMED last updated this device on Oct 15, 2025

SinaVita® Immune Support Oral Spray

735017801073501780100776V

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MIM Pharma Europe AB
UDI-DI code: 07350178010077
Reference / catalog number: MIM-IMM-OS-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

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

CW275
Consult your healthcare provider if pregnant, breastfeeding or on medication.
CW011
Do not use if allergic to any ingredient.
CW999
Full list of warnings and contraindications available in the Instructions for Use (IFU).

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Market distribution

Primary placement in Norway; available across 2 countries total.

Country	On market since	Until
NorwayPrimary placement	Nov 15, 2025	Still on market
Sweden	Nov 15, 2025	Still on market

Device identification

Trade name: SinaVita® Immune Support Oral Spray
UDI-DI code: 07350178010077
Basic UDI-DI: 735017801073501780100776V
Reference / catalog number: MIM-IMM-OS-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 Class I medical device intended for home use as an oral spray to moisten and soothe the oral and oropharyngeal mucosa, supporting immune resilience and comfort during cold and flu season. Designed to maintain the normal protective function of the mucous membranes and ease seasonal throat discomfort. Multi-dose, external use only. Not a medicinal product.
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)07350178010077

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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.

Q030103NASAL IRRIGATION SOLUTIONS

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.