Organization name

TOPCON CORPORATION

SRN

JP-MF-000003928

Manufacturer status

Active

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

• CW011

  • To avoid injury of the patient, be careful not to bump the patient's eye or nose with the instrument when operating the touch display. • Mount the ANTERIOR ATTACHEMENT HA-2 on the forehead rest securely. Otherwise, the attachment may come off during photography and the patient may be injured. • To avoid injury of the patient, be careful not to bump the patient's eye or nose with the Anterior segment lens unit when operating the control lever.
• CW999

  NOTE: • Mount the ANTERIOR ATTACHEMENT HA-2 on the forehead rest securely. If not, the anterior segment photography is not possible. • Do not bend the ANTERIOR ATTACHEMENT HA-2 forcedly. It may be broken or deformed.

Primary placement in Netherlands; available across 31 countries total.

Trade name

ANTERIOR SEGMENT ATTACHMENT KIT AA-1

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.

04571130282193

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.

4560126260041U5

Reference / catalog number

AA-1

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 I

Applicable legislation

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

Status

On the market

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.

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

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

• Z12120121OPTICAL CONSISTENCY TOMOGRAPHS

• Class I medical devices in EUDAMED

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