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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Philips Neuro Coil PMS — 7 UDI-DI variants, MDR

MD Atlas
Philips Medical Systems Nederland B.V.

Data from EUDAMED, last updated May 30, 2026

Philips Neuro Coil PMS

0884838BM912TE

7 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Philips Medical Systems Nederland B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0884838BM912TE
Device name: Philips Neuro Coil PMS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Philips Medical Systems Nederland B.V.
SRN: NL-MF-000001489
Country: Netherlands
Email: eudamed@philips.com
Phone: n/a

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01JJT5A2J8JG75Q15844B843DP

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

DS BASE 1.5T00884838118065
DS Base 3.0T00884838118089
DS Head 1.5T00884838118058
DS Head 3.0T00884838118096
dS Head 32CH 3.0T00884838118119
DS HeadNeck 1.5T00884838118072
DS HeadNeck 3.0T00884838118102