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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.

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BPOM Registered
Risk Class Kelas Resiko : C
Nexsphere-F ™
Analysis ID: AKL 20503420148

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. FONDA MEDIKA MAIN

AR 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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