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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

OK NIGHT PRESBYO — Class IIa MDR by MEDLAC S.r.l.

MD Atlas
MEDLAC S.r.l.

EUDAMED last updated this device on Feb 21, 2026

OK NIGHT PRESBYO

805221198LACORTOKU7

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDLAC S.r.l.
UDI-DI code: 08052211980062
Reference / catalog number: OK NIGHT PRESBYO

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View device family (Basic UDI)

Manufacturer information

Organization name: MEDLAC S.r.l.
SRN: IT-MF-000030386
Manufacturer status: Active

Related devices

OK NIGHT (EM)805221198LACORTOKU7On the market OK NIGHT (TOP)805221198LACORTOKU7On the market OK NIGHT (TR)805221198LACORTOKU7On the market OK NIGHT (MOONLENS)805221198LACORTOKU7On the market OK NIGHT (GOV)805221198LACORTOKU7On 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	Feb 21, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08052211980062
Basic UDI-DI: 805221198LACORTOKU7
Reference / catalog number: OK NIGHT PRESBYO
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.

Q02100499CONTACT LENSES - OTHER

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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