MD Atlas
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Data last updated: Apr 2025
CardIQ Fusion SPECT
8406821BUG00064H6
On Market
Class IIa
Regulation
EU MDR
Manufacturer
GE Medical Systems SCS
Primary DI
00195278688484
Reference
5934730
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Identification
Primary DI
00195278688484
Basic UDI-DI
8406821BUG00064H6
Reference
5934730
Issuing Agency
—
ULID
J24KXKAX
Classification
Risk Class
Class IIa
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
GE Medical Systems SCS
Manufacturer SRN
FR-MF-000000687
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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