Organization name

Agfa NV

SRN

BE-MF-000000571

Manufacturer status

Active

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

• P281 – Use personal protective equipment as required.
• EUH 401 – To avoid risks to human health and the environment, comply with the instructions for use.

Primary placement in Belgium; available across 32 countries total.

Trade name

DR 800

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.

05414904251805

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.

5414904272824YK

Reference / catalog number

XCTMA

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 IIb

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.

• Z11030702DIGITAL REMOTE CONTROL TABLES

• Class IIb medical devices in EUDAMED

• 28620125060Supplemented
  Quality management systemNotified body: Intertek Medical Notified Body AB (2862)Expiry: May 31, 2027

Certificate health across this manufacturer's portfolio.