EUDAMED last updated this device on Aug 27, 2025

VisOcu HPMC

425090620HM-OVDYL

On the marketClass IIb

Applicable legislation: —
Organization name: Phibio GmbH
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04250906200011
Reference / catalog number: PHI202DE-VSOH

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

VisOcu HPMC is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Phibio GmbH. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: VisOcu HPMC
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04250906200011
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: 425090620HM-OVDYL
Reference / catalog number: PHI202DE-VSOH
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class IIb
Applicable legislation: —
Status: On the market

Device details

Quantity: 50
Additional product description: Opthalmic Viscosurgical Device-HPMC
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)04250906200011

UDI-PI DataMatrix

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

EMDN nomenclature code(s)

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

Q02030301OPHTHALMOLOGY, HYALURONIC ACID AND DERIVATIVES

Critical warnings

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

Caution
Consult instructions for use
See instructions for use
Do not re-use
Do not resterilize
Do not re-sterilise

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in France; available across 3 countries total.

Country	On market since	Until
FrancePrimary placement	—	Still on market
Germany	—	Still on market
EL	—	Still on market

VisOcu HPMC

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates covering this device

Related devices

Certificates