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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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EarliQ — 4 UDI-DI variants, MDR (NVV Pharma B.V.)

MD Atlas
NVV Pharma B.V.

Data from EUDAMED, last updated May 31, 2026

EarliQ

8721161755E010XXRU

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: NVV Pharma B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8721161755E010XXRU
Device name: EarliQ
Device model: Drops (E010XX), Drops & Syringe (E20XX), Spray (E30XX, E40XX, E50XX, E60XX)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: NVV Pharma B.V.
SRN: NL-MF-000043888
Country: Netherlands
Email: info@nvvpharma.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K3130ETGHY6B70E9A3MJ034A

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ClearliQ Earwax Drops & Syringe08721161755210
ClearliQ Earwax Spray08721161755227
Kruidvat Gouttes Cérumen08721161755005
Kruidvat Spray Cérumen 4-en-108721161755036