Pure Global

SCARCLINIC ™ Clear - Indonesia BPOM Medical Device Registration

SCARCLINIC ™ Clear is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603420793. The device is manufactured by HANSBIOMED CORP. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
SCARCLINIC ™ Clear
Analysis ID: AKL 11603420793

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

HANSBIOMED CORP.

Country of Origin

Korea

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Apr 06, 2024

Expiry Date

Nov 27, 2028

Product Type

Surgical Equipment

Silicone sheeting.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing