CG500

by Philips Healthcare (Suzhou) Co., Ltd. 3 variants

Ref 300009349691

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number0884838BM954TW Basic UDI-DI 00884838118447UDI-DI	Date31 Jul 2024Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: CG500 Product family Base model
Model / Reference: 300009349691

Primary DI / UDI-DI: 00884838118447
Basic UDI-DI: 0884838BM954TW
Direct Marketing DI: 00884838118447
EMDN Code: Z11039011 High voltage x-ray generators

Device Class: Class IIb
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000003923
Authorised representative: Philips Medical Systems Nederland B.V. NL-AR-000001422

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No