Nexsphere-F ™ - Indonesia BPOM Medical Device Registration
Nexsphere-F ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503420148. The device is manufactured by NEXTBIOMEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FONDA MEDIKA MAIN.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
NEXTBIOMEDICAL CO., LTD.Country of Origin
Korea
Authorized Representative
PT. FONDA MEDIKA MAINAR Address
Ruko Roxy Mas Blok C4 No. 1-2, JL. KH Hasyim Ashari No.125
Registration Date
Oct 07, 2024
Expiry Date
Jul 12, 2027
Product Type
Prosthetic Cardiology Equipment
Vascular embolization device
Non Electromedic Sterile
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