DS Base 3.0T

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.

• CW014

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

  EUDAMED did not publish a description for this code.
• CW025

  EUDAMED did not publish a description for this code.

Primary placement in Netherlands; available across 23 countries total.

Trade name

DS Base 3.0T

UDI-DI code

00884838118089

Basic UDI-DI

0884838BM912TE

Reference / catalog number

459801730062

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

"dS NVS Head Base coil is part of dS NVS coil.. dS NVS Coil consists of the following light weight coils integrated to work seamlessly as a single integrated coil: • dS NVS Head Base • dS NVS Head Top • dS NVS Spine The i

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
• Z1105018002MAGNETIC RESONANCE (MR) RADIOFREQUENCY VOLUMETRIC COILS
• Z1105018001MAGNETIC RESONANCE (MR) RADIOFREQUENCY SURFACE COILS