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Organization name
UDI-DI code
Reference / catalog number

M0188 — Class IIa MDR by Neupharma srl

MD Atlas
Neupharma srl

Manufacturer information

Organization name: Neupharma srl
SRN: IT-MF-000027967
Manufacturer status: Active

Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030056-00Issued
Quality management systemNotified body: 0425Expiry: Nov 22, 2028

Related devices

This device is not currently linked to any other device.

EUDAMED last updated this device on Mar 21, 2024

M0188

805140656NARIDEKBAGWJ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Neupharma srl
UDI-DI code: 08051406560171
Reference / catalog number: M0188

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View device family (Basic UDI)

Manufacturer information

Organization name: Neupharma srl
SRN: IT-MF-000027967
Manufacturer status: Active

Critical warnings

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

CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Nov 23, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08051406560171
Basic UDI-DI: 805140656NARIDEKBAGWJ
Reference / catalog number: M0188
Issuing entity: GS1

Classification

Risk category: Class IIa
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

EMDN nomenclature code(s)

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

Q030103NASAL IRRIGATION SOLUTIONS

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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Related devices

This device is not currently linked to any other device.

Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030056-00Issued
Quality management systemNotified body: 0425Expiry: Nov 22, 2028