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RUIKD INFIUTH Hifu - Indonesia BPOM Medical Device Registration

RUIKD INFIUTH Hifu is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603812232. The device is manufactured by RUIKD KOREA LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BCS PRIMA INDONESIA.

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
RUIKD INFIUTH Hifu
Analysis ID: AKL 21603812232

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

RUIKD KOREA LTD.

Country of Origin

Korea

Authorized Representative

PT. BCS PRIMA INDONESIA

AR Address

Jl. Pondok Kopi Raya Blok A No. 8 RT 009 RW 010

Registration Date

Dec 30, 2022

Expiry Date

Aug 18, 2027

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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