MR-RT CouchTop

Organization name

Philips Medical Systems Nederland B.V.

SRN

NL-MF-000001489

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW016

  EUDAMED did not publish a description for this code.
• CW018

  EUDAMED did not publish a description for this code.
• CW999

  Type B applied part Defibrillation-proof type B applied part

Primary placement in Netherlands; available across 32 countries total.

Trade name

MR-RT CouchTop

UDI-DI code

00884838112759

Basic UDI-DI

0884838BM952TS

Reference / catalog number

459800573515

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

MR-RT is an add-on to the existing Ingenia 1.5T and 3.0T MR systems that makes the system suitable for MR imaging for radiation therapy planning purposes. MR-RT consists of RTGo SW and MR CouchTop accessory. RTgo is a softwar

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