Organization name

VitreQ B.V.

SRN

NL-MF-000000424

Manufacturer status

Active

Primary placement in Netherlands; available across 32 countries total.

Trade name

not provided

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

08719214223298

Basic UDI-DI

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.

871921422999H2

Reference / catalog number

VT25.D02

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

5

Additional product description

The device is intended for the removal (nibble away) of vitreous humour and vitreal membranes during ophthalmic surgery in the posterior segment of the eye or in case of posterior capsule rupture to remove the vitreous humour out of the anterior segment of the eye.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• Z1212020703VITRECTOMES

• Class IIa medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.