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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

C.N. 182225.3 — Class IIb MDR by Farmamix Visión S.L.

MD Atlas
Farmamix Visión S.L.

EUDAMED last updated this device on Nov 25, 2025

C.N. 182225.3

8437022534008IVISIONXD

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Farmamix Visión S.L.
UDI-DI code: 08437022534015
Reference / catalog number: C.N. 182225.3

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Manufacturer information

Organization name: Farmamix Visión S.L.
SRN: ES-MF-000028718
Manufacturer status: Active

Critical warnings

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

CW275
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437022534015
Basic UDI-DI: 8437022534008IVISIONXD
Reference / catalog number: C.N. 182225.3
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: iVision Dry multidose 10 ml is a sterile topic ophthalmic solution of physiological pH, hypo-osmolar, free of preservatives and phosphates. iVision Dry 10 ml is suitable for contact lenses
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q02030206EYE LUBRICANT 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

C.N. 182224.68437022534008IVISIONXDOn 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.