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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

Kruidvat Gouttes Cérumen — Class I MDR by NVV Pharma B.V.

MD Atlas
NVV Pharma B.V.

EUDAMED last updated this device on Apr 13, 2026

Kruidvat Gouttes Cérumen

8721161755E010XXRU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NVV Pharma B.V.
UDI-DI code: 08721161755005
Reference / catalog number: E010NL

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View device family (Basic UDI)

Manufacturer information

Organization name: NVV Pharma B.V.
SRN: NL-MF-000043888
Manufacturer status: Active

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ClearliQ Earwax Drops & Syringe8721161755E010XXRUOn the market ClearliQ Earwax Spray8721161755E010XXRUOn the market Kruidvat Spray Cérumen 4-en-18721161755E010XXRUOn the market

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.

Critical warnings

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

CW275
Consult your doctor or pharmacist before using this product if you are pregnant or breastfeeding or when you suffer from an ear infection.
CW135
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.
CW999
Do not use in case of: - damaged or perforated eardrums, grommets, (ear tubes), open wounds (for example, after ear surgery) or when the ear canal is blocked by a foreign object. - When you are hypersensitive or allergic to any of the ingredients. Consult a doctor if you experience pain, persistent irritation, or an allergic reaction.

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Market distribution

Primary placement in Netherlands; available across 2 countries total.

Country	On market since	Until
NetherlandsPrimary placement	Oct 17, 2025	Jan 1, 2035
Belgium	Oct 17, 2025	Jan 1, 2035

Device identification

Trade name: Kruidvat Gouttes Cérumen
UDI-DI code: 08721161755005
Basic UDI-DI: 8721161755E010XXRU
Reference / catalog number: E010NL
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: —
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)08721161755005

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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.

Q03040201EAR DROPPERS

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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