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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

4503 — Class I MDR by Centrofarc S.p.A

MD Atlas
Centrofarc S.p.A

EUDAMED last updated this device on Aug 22, 2025

4503

805329520NIT00MISSGLOVENV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Centrofarc S.p.A
UDI-DI code: 08053295200046
Reference / catalog number: 4503

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View device family (Basic UDI)

Manufacturer information

Organization name: Centrofarc S.p.A
SRN: IT-MF-000047697
Manufacturer status: Active

Related devices

4508805329520NIT00MISSGLOVENVOn the market 4507805329520NIT00MISSGLOVENVOn the market 4509805329520NIT00MISSGLOVENVOn the market 4516805329520NIT00MISSGLOVENVOn the market 4515805329520NIT00MISSGLOVENVOn 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.

CW011
Non ingerire. Tenere lontano dalla portata di bambini e animali.

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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: 08053295200046
Basic UDI-DI: 805329520NIT00MISSGLOVENV
Reference / catalog number: 4503
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: Disposable, non-sterile nitrile gloves. Latex-free, powder-free, matte blue color, ambidextrous with tear-resistant cuff. Micro-rough surface designed to ensure maximum sensivity for an optimized grip.
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)08053295200046

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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.

T01020204NITRILE EXAMINATION / TREATMENT GLOVES

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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