EUDAMED last updated this device on Feb 6, 2026

NHD-S-1

805452935NHDLP

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOSS S.p.A.
UDI-DI code: 08054529350438
Reference / catalog number: NHD-S-1

NHD-S-1 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by MOSS S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

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Country
Date of registration
Address

EUDAMED last updated this device on Feb 6, 2026

NHD-S-1

805452935NHDLP

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOSS S.p.A.
UDI-DI code: 08054529350438
Reference / catalog number: NHD-S-1

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 08054529350438
Basic UDI-DI: 805452935NHDLP
Reference / catalog number: NHD-S-1
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)08054529350438

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

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

M040413INTERACTIVE DRESSINGS

Critical warnings

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

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

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

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: 08054529350438
Basic UDI-DI: 805452935NHDLP
Reference / catalog number: NHD-S-1
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.

Manufacturer information

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08054529350438

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

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

M040413INTERACTIVE DRESSINGS

Critical warnings

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

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

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

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

Legacy certificates

Certificate number: EPT 0477.MDR.22/4952
Type: Quality management system
Notified body: Eurofins Product Testing Italy S.r.l. (0477)
Validity: Oct 7, 2022 → Oct 6, 2027

Certificates covering this device

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

All products by MOSS S.p.A.

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

NHD-S-1

NHD-S-1

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Legacy certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Legacy certificates

Certificates covering this device

Related devices