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Organization name
UDI-DI code
Reference / catalog number

ViscOge — Class IIb MDR by Phibio GmbH

MD Atlas
Phibio GmbH

EUDAMED last updated this device on Aug 27, 2025

ViscOge

425090620HA-OVDUG

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Phibio GmbH
UDI-DI code: 04250906200165
Reference / catalog number: PHI301DE-VSG

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Manufacturer information

Organization name: Phibio GmbH
SRN: DE-MF-000045435
Manufacturer status: Active

Critical warnings

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

CW011
Caution
CW010
See instructions for use
CW009
Do not re-use
CW001
Do not re-sterilise

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

Device identification

Trade name: ViscOge
UDI-DI code: 04250906200165
Basic UDI-DI: 425090620HA-OVDUG
Reference / catalog number: PHI301DE-VSG
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: 50
Additional product description: Opthalmic Viscosurgical Device
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q02030301OPHTHALMOLOGY, HYALURONIC ACID AND DERIVATIVES

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

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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.