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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

1 — Class I MDD by Natur Produkt Zdrovit…

MD Atlas
Natur Produkt Zdrovit Sp. z o.o.

EUDAMED last updated this device on May 25, 2026

1

B-5902026467674Z3

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Natur Produkt Zdrovit Sp. z o.o.
UDI-DI code: D-5902026467674Z3
Reference / catalog number: 1

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View device family (Basic UDI)

Manufacturer information

Organization name: Natur Produkt Zdrovit Sp. z o.o.
SRN: PL-MF-000010540
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-5902026467674Z3
Basic UDI-DI: B-5902026467674Z3
Reference / catalog number: 1
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: ear spray
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

D-5902026467674Z3

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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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Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

TNP/MDR/0048/5905/2026Issued
Quality management systemNotified body: 2274Expiry: Feb 12, 2029