Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

geneMAP

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
D-TRMF000028405SMN1MRT5J5
Basic UDI-DI Code
B-TRMF000028405SMN1MRT5J5
Reference
SMN1M-RT50
Device Types
None provided
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

Spinal Muscular Atrophy (SMA), progressive degeneration of the spinal cord and brainstem nuclei and anterior It is a disease characterized by muscle weakness and atrophy resulting from the loss of horn cells. SMA is an autosomal recessive disorder caused by mutations in the SMN1 (Survival Motor Neuron) gene. is a disease. Approximately 94% of SMA patients can be detected by commonly used molecular assays. SMN1 lacks both copies of exons 7 and 8, while carrier individuals have one copy

CND Nomenclature Codes

Code Description
W0106010199 MONOGENETIC DISORDERS TESTS - OTHER

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