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CUVIS-Joint - Indonesia BPOM Medical Device Registration

CUVIS-Joint is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002320130. The device is manufactured by CUREXO INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SKBIO NUSA MEDICA.

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 : B
CUVIS-Joint
Analysis ID: AKL 21002320130

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CUREXO INC.

Country of Origin

Korea

Authorized Representative

PT. SKBIO NUSA MEDICA

AR Address

KOMPLEK WIJAYA GRAHA PURI BLOK G NO. 17 LT. 3 JL. WIJAYA II, KEL. PULO KEC. KEBAYORAN BARU JAKARTA SELATAN

Registration Date

Apr 19, 2023

Expiry Date

Dec 21, 2027

Product Type

Surgical Neurology Equipment

Stereotaxic instrument.

Non Radiation Electromedics

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