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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

C941662633 — Class IIa MDR by Eye Pharma S.p.a.

MD Atlas
Eye Pharma S.p.a.

EUDAMED last updated this device on Dec 23, 2025

C941662633

805957143REXF

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Eye Pharma S.p.a.
UDI-DI code: 08059571430053
Reference / catalog number: C941662633

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View device family (Basic UDI)

Manufacturer information

Organization name: Eye Pharma S.p.a.
SRN: IT-MF-000026349
Manufacturer status: Active

Related devices

A941662633805957143REXFOn the market A942891615805957143REXFOn the market C940223910805957143REXFOn the market C942891615805957143REXFOn the market A940223910805957143REXFOn the market

Critical warnings

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

CW010
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		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08059571430053
Basic UDI-DI: 805957143REXF
Reference / catalog number: C941662633
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)08059571430053

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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.

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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Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030167-00Issued
Quality management systemNotified body: 0425Expiry: Dec 21, 2030