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HKT Curette - Indonesia BPOM Medical Device Registration

HKT Curette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303915208. The device is manufactured by HANKIL TECH MEDICAL CO., LTD. from Korea, Democratic People's Republic Of, and is classified as Risk Class Kelas Resiko : A. 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 : A
HKT Curette
Analysis ID: AKL 11303915208

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea, Democratic People's Republic Of

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

Feb 17, 2024

Expiry Date

Jan 31, 2029

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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