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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

KT-001-2026 — Class I MDR by VERCO S.A.

MD Atlas
VERCO S.A.

EUDAMED last updated this device on Feb 23, 2026

KT-001-2026

590619043kompresnaoczyA9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VERCO S.A.
UDI-DI code: 05906190439338
Reference / catalog number: KT-001-2026

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Manufacturer information

Organization name: VERCO S.A.
SRN: PL-MF-000034196
Manufacturer status: Active

Critical warnings

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

CW007
Nie używać jeśli opakowanie zostało uszkodzone
CW010
Przed użyciem należy zapoznać się instrukcją używania
CW999
Nie stosować na podrażnioną, zaczerwienioną, swędzącą skórę, na otwarte rany lub gdy odczuwanie ciepła lub zimna jest zaburzone. Nie stosować w przypadku naruszonej hermetyczności wyrobu. Przed każdym użyciem wyrobu należy sprawdzić jego szczelność. Stosowanie wyrobu u dzieci wyłącznie pod nadzorem osoby dorosłej, która odpowiada za bezpieczne używanie wyrobu podczas terapii ciepłem lub zimnem

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Market distribution

Primary placement in Poland; available across 1 country total.

Placed on the market in Poland; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05906190439338
Basic UDI-DI: 590619043kompresnaoczyA9
Reference / catalog number: KT-001-2026
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: Demoxoft Kompres termiczny na oczy stanowi wyrób medyczny wielokrotnego użytku stosowany do terapii ciepłem lub zimnem na okolicę oczu.
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)05906190439338

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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.

M9001CRYOTHERAPY AND THERMOTHERAPY DEVICES

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

This device is not currently linked to any other device.

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.