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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

LinfoVir IsoWash — Class IIa MDR by NOOS S.r.l.

MD Atlas
NOOS S.r.l.

EUDAMED last updated this device on Feb 12, 2024

LinfoVir IsoWash

805210720LVIRIPERWASH6A

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NOOS S.r.l.
UDI-DI code: 08052107200380
Reference / catalog number: LinfoVir IsoWash

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View device family (Basic UDI)

Manufacturer information

Organization name: NOOS S.r.l.
SRN: IT-MF-000027739
Manufacturer status: Active

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: 08052107200380
Basic UDI-DI: 805210720LVIRIPERWASH6A
Reference / catalog number: LinfoVir IsoWash
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

UDI-DI DataMatrix

Encoded

(01)08052107200380

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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.

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

LinfoVir IsoWash805210720LVIRIPERWASH6AOn the market LinfoVir IperWash805210720LVIRIPERWASH6AOn the market LinfoVir IperWash 805210720LVIRIPERWASH6AOn the market LINFOVIR PLUS GOCCE NASALI 805210720LVIRPLUSZGOn the market LINFOVIR PLUS SPRAY NASALE805210720LVIRPLUSZGOn the market

Certificates

Certificate health across this manufacturer's portfolio.

039-00-00-MDRIssued
Quality management systemNotified body: 0426Expiry: Jan 23, 2029