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Brilliance iCT

FDA UDIEUDAMED

Class II (US FDA UDI)

by Philips Medical Systems Nederland B.V.

Identity

Trade Name
Brilliance iCT FDA UDI
Generic Name
Full-body CT system FDA UDI
Model / Reference
Brilliance iCT SP FDA UDI

Identifiers

Catalog Number
728311 FDA UDI
Primary DI / UDI-DI
00884838059481 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
Full-body CT system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Full-body CT system

Brilliance iCT by Philips Medical Systems Nederland B.V. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Full-body CT system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 987d7e77-8588-49d2-a287-555d3916dcba 33 fields · synced Sep 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026