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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

NPKLb-IT — Class IIb MDR by MOSS S.p.A.

MD Atlas
MOSS S.p.A.

EUDAMED last updated this device on Apr 27, 2026

NPKLb-IT

805452935NTPNK

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOSS S.p.A.
UDI-DI code: 08054529350636
Reference / catalog number: NPKLb-IT

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View device family (Basic UDI)

Manufacturer information

Organization name: MOSS S.p.A.
SRN: IT-MF-000010071
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW032
Expiry date - yyyy/mm/dd
CW999
Read warnings prior to use

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Oct 7, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08054529350636
Basic UDI-DI: 805452935NTPNK
Reference / catalog number: NPKLb-IT
Issuing entity: GS1

Classification

Risk category: Class IIb
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)08054529350636

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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.

M040413INTERACTIVE DRESSINGS

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

Certificate health across this manufacturer's portfolio.

EPT 0477.MDR.22/4951Issued
Quality management systemNotified body: 0477Expiry: Oct 6, 2027
EPT 0477.MDR.22/4952Issued
Quality management systemNotified body: 0477Expiry: Oct 6, 2027