Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

025 — Class IIa MDR by OPTILAB S.R.L.

MD Atlas
OPTILAB S.R.L.

EUDAMED last updated this device on May 12, 2026

025

805750736A02FX

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OPTILAB S.R.L.
UDI-DI code: 08057507360313
Reference / catalog number: 025

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

Organization name: OPTILAB S.R.L.
SRN: IT-MF-000026824
Manufacturer status: Active

Related devices

023805750736A02FXOn the market 025805750736A02FXOn the market 021805750736A02FXOn the market 023805750736A02FXOn the market 025805750736A02FXOn the market

Certificates

Certificate health across this manufacturer's portfolio.

066/MDRIssued
Quality assuranceNotified body: 0051Expiry: Dec 20, 2027

Critical warnings

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

CW010
Bugiardino per lente a contatto annuale idrofila
CW030
seguire sempre le istruzioni dello specialista di settore.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Dec 21, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08057507360313
Basic UDI-DI: 805750736A02FX
Reference / catalog number: 025
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: lente a contatto morbida annuale bio gel multifocale 45% idrofilia.
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)08057507360313

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

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

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

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

Q0210040102CONTACT LENSES - HYDROGEL, REUSABLE

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

Become a partner of MD Atlas