- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 24, 2026
0884838BM1050LQCT ASPECT Scoring is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Philips Medical Systems Nederland B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
00884838129993881093NL-MF-000001489(01)00884838129993
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
CW999Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Netherlands; available across 6 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jul 1, 2026 | Still on market |
| Belgium | Jul 1, 2026 | Still on market |
| Spain | Jul 1, 2026 | Still on market |
| France | Jul 1, 2026 | Still on market |
| Ireland | Jul 1, 2026 | Still on market |
| Luxembourg | Jul 1, 2026 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z11069082VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - SOFTWARE ACCESSORIESPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →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.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →0884838BM798U8On the marketCerebral Filter0884838BM801T4On the marketCT ASPECT Scoring0884838BM1050LQOn the marketdS 1.5T 1CH Lateral Left0884838BM914TJOn the marketdS 1.5T 1CH Lateral Right0884838BM914TJOn the marketdS 1.5T 4CH Lateral Left0884838BM914TJOn the marketCertificate health across this manufacturer's portfolio.
HZ 1135905-1SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →No certificate specifically references this device's Basic UDI-DI.