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Organization name
UDI-DI code
Reference / catalog number

6601040 — Class I MDD by Ursatec GmbH

MD Atlas
Ursatec GmbH

EUDAMED last updated this device on May 8, 2026

6601040

B-6601040XT

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Ursatec GmbH
UDI-DI code: D-6601040XT
Reference / catalog number: 6601040

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Manufacturer information

Organization name: Ursatec GmbH
SRN: DE-MF-000005353
Manufacturer status: Active

Critical warnings

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

CW999
Als de Kruidvat Neusspray met 0,9% zeezout correct wordt gebruikt zijn er geen speciale waarschuwingen en voorzorgsmaatregelen nodig. Om de hygiëne te waarborgen mag het fiesje neusspray maar door een en dezelfde persoon worden gebruikt. Kruidvat Neusspray met 0,9% zeezout moet worden gebruikt bij kamertemperatuur. De uiterste gebruiksdatum van Kruidvat Neusspray met 0,9% zeezout staat op het doosje en etiket van het flesje. U mag de Kruidvat Neusspray met 0,9% zeezout niet meer gebruiken na afloop van de uiterste gebruiksdatum. Kruidvat Neusspray met 0,9% zeezout moet op een temperatuur van minder dan 25°C worden bewaard. Buiten het bereik van kinderen houden. Er zijn geen bekende bijwerkingen. Er zijn geen bekende contra-indicaties. Er zijn geen bekende wisselwerkingen.

Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-6601040XT
Basic UDI-DI: B-6601040XT
Reference / catalog number: 6601040
Issuing entity: EUDAMED

Classification

Risk category: Class I
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)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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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.