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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

Cellulose wadding hygienic sheets — Class I MDR

MD Atlas
GRIGEO TISSUE Sp. z o.o.

EUDAMED last updated this device on Feb 29, 2024

Cellulose wadding hygienic sheets

590735400watawarkuszachNH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GRIGEO TISSUE Sp. z o.o.
UDI-DI code: 05907354001798
Reference / catalog number: 41-0-2-10-280

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View device family (Basic UDI)

Manufacturer information

Organization name: GRIGEO TISSUE Sp. z o.o.
SRN: PL-MF-000040115
Manufacturer status: Active

Critical warnings

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

CW011
Wyrób nie jest przeznaczony do kontaktu z uszkodzoną skórą!

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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: Cellulose wadding hygienic sheets
UDI-DI code: 05907354001798
Basic UDI-DI: 590735400watawarkuszachNH
Reference / catalog number: 41-0-2-10-280
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: 5
Additional product description: Do celów higienicznych w gabinetach zabiegowych, salach szpitalnych, w celu zabezpieczenia przed wydzielinami i wydalinami od pacjentów personelu medycznego oraz innych pacjentów. Wata celulozowa dzięki wysokim właściwościom chłonnym jest wyrobem medycznym, który służy do odsączania wydzielin (np. ślina), powycierania i zaabsorbowania rozlanych płynów (np. wymiociny). Wata celulozowa może być zamiennikiem podkładów higienicznych dla pacjentów przy zabiegach
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 40–60 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05907354001798

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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.

T0306PATIENT PROTECTION DEVICES DURING CLINICAL PROCEDURES

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.