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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

00052 — Class I MDR by Turati Idrofilo S.p.A.

MD Atlas
Turati Idrofilo S.p.A.

EUDAMED last updated this device on Mar 30, 2026

00052

8023546COTTONWJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Turati Idrofilo S.p.A.
UDI-DI code: 08023546000527
Reference / catalog number: 00052

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View device family (Basic UDI)

Manufacturer information

Organization name: Turati Idrofilo S.p.A.
SRN: IT-MF-000045672
Manufacturer status: Active

Related devices

000618023546COTTONWJOn the market 000548023546COTTONWJOn the market 000518023546COTTONWJOn the market 000568023546COTTONWJOn the market 900118023546COTTONWJOn the market

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.

Critical warnings

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

CW999
Non ingerire, evitare usi impropri, non utilizzare su cute lesa o mucose

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08023546000527
Basic UDI-DI: 8023546COTTONWJ
Reference / catalog number: 00052
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: —
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)08023546000527

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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.

M010101HYDROPHILIC COTTON

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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