Organization name

Philips Medical Systems Nederland B.V.

SRN

NL-MF-000001489

Manufacturer status

Active

Primary placement in Netherlands; available across 32 countries total.

Trade name

Trolley

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.

00884838099487

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.

0884838BM474TB

Reference / catalog number

989603008226

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

The Patient Trolley Frame is a stainless steel frame with four wheels for easy transportation of the patient positioned on the system's tabletop.

Additional information URL

https://www.philips.nl/healthcare/over-ons/support/resource-center/results#sort=relevancy&f:@ps_contenttype=[Instruction%20for%20Use]&f:@ps_modality=[Magnetic%20resonance%20(MRI)]&f:@ps_language=[English%20(US)]

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.

• Z1105018099MAGNETIC RESONANCE (MR) SYSTEMS - HARDWARE ACCESSORIES - OTHER

• Class I medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

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