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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

KHC 1 — Class I MDR by "JOHN COTTON EUROPE"…

MD Atlas
"JOHN COTTON EUROPE" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

EUDAMED last updated this device on Nov 27, 2025

KHC 1

5905428KHC13Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: "JOHN COTTON EUROPE" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
UDI-DI code: 05905428044634
Reference / catalog number: KHC 1

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View device family (Basic UDI)

Manufacturer information

Organization name: "JOHN COTTON EUROPE" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000027273
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.

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

Device identification

Trade name: not provided
UDI-DI code: 05905428044634
Basic UDI-DI: 5905428KHC13Z
Reference / catalog number: KHC 1
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: Kołdra służy do przykrywania ciała w celu zapewnienia ciepła i izolacji cieplnej, podczas odpoczynku lub snu, u osób cierpiących na alergie (alergików) i osób zdrowych. Kołdra wykonana jest z materiałów barierowych (podłoże poliestrowe), które uniemożliwiają namnażanie się roztoczy kurzu domowego, głównego alergenu człowieka. Wyrób umożliwia unikanie lub ograniczenie ekspozycji na te alergeny, dzięki temu może być stosowany wspomagająco w zapobieganiu i łagodzeniu przebiegu niektórych chorób alergicznych.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 220 x 200 cm

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05905428044634

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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.

Y1899AIDS, FURNITURE AND HOME AIDS FOR PERSONS WITH DISABILITIES - OTHER

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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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.