ECLIPSE 2L - Indonesia BPOM Medical Device Registration
ECLIPSE 2L is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420505. The device is manufactured by BALT EXTRUSION SAS from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDIKON MAIN PHARMALAB.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BALT EXTRUSION SASCountry of Origin
France
Authorized Representative
MEDIKON MAIN PHARMALABAR Address
JLN. RAYA PASAR MINGGU NO 15, RT.001/07
Registration Date
Sep 27, 2024
Expiry Date
Dec 31, 2027
Product Type
Diagnostic Cardiology Equipment
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RANGE
SILK VISTA Intracranial Self Expandable Stent
FARGO MINI Guiding Catheter
VASCO+ Microcatheter
MAGIC Microcatheter for Detachable Balloons
BALT SILK+ Intracranial Self Expandable Stent and Delivery System
BALT EXTRUSION SAS
LEO + BABY Intracranial Self Expandable Stent
BALT EXTRUSION SAS
RANGE
BALT EXTRUSION SAS
SILK VISTA Intracranial Self Expandable Stent
BALT EXTRUSION SAS
FARGO Guiding Catheters
BALT EXTRUSION SAS.
FARGO MINI Guiding Catheter
BALT EXTRUSION SAS
VASCO+ Microcatheter
BALT EXTRUSION SAS
MAGIC Microcatheter for Detachable Balloons
BALT EXTRUSION SAS
MAGIC Microcatheter
BALT EXTRUSION SAS
HYBRID Wire Hydrophilic Guidewire
BALT EXTRUSION SAS