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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

NebuMar — Class IIa MDD by Merckle GmbH

MD Atlas
Merckle GmbH

EUDAMED last updated this device on Nov 6, 2025

NebuMar

B-269955RQ

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Merckle GmbH
UDI-DI code: D-269955RQ
Reference / catalog number: 269955

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Manufacturer information

Organization name: Merckle GmbH
SRN: DE-MF-000018230
Manufacturer status: Active

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Critical warnings

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

CW135
EUDAMED did not publish a description for this code.
CW277
EUDAMED did not publish a description for this code.
CW276
n case concomitant use of nasal medicinal products is necessary, please contact your doctor or pharmacist
CW999
En caso de que sea necesario utilizar simultáneamente medicamentos administrados por vía nasal, consulte a su médico o farmacéutico
CW999
Report any serious incident that occur in relation to the device to the manufacturer and the competent authority.
CW999
Do not use NebuMar Nasal Congestion spray for more than 30 consecutive days.
CW999
Use only for the intended purpose.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 8, 2013	Aug 31, 2026

Device identification

Trade name: NebuMar
UDI-DI code: D-269955RQ
Basic UDI-DI: B-269955RQ
Reference / catalog number: 269955
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC 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.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.