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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

NWCV0153 — Class I MDR by DEALFA S.r.l.

MD Atlas
DEALFA S.r.l.

EUDAMED last updated this device on May 18, 2026

NWCV0153

805576595T0207B9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DEALFA S.r.l.
UDI-DI code: 18055765952407
Reference / catalog number: NWCV0153

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View device family (Basic UDI)

Manufacturer information

Organization name: DEALFA S.r.l.
SRN: IT-MF-000021998
Manufacturer status: Active

Related devices

NWCSM003805576595T0204017POn the market NWCB0154805576595T0207B9On the market NWCV0151805576595T0207B9On the market NWCB0153805576595T0207B9On the market NWCPE001805576595T0208BBOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 18055765952407
Basic UDI-DI: 805576595T0207B9
Reference / catalog number: NWCV0153
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: 100
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

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

T0207CAPS AND HEADWEAR (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE)

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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