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LINEARZ Focused Ultrasound Stimulator System - Indonesia BPOM Medical Device Registration

LINEARZ Focused Ultrasound Stimulator System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324416. The device is manufactured by JEISYS MEDICAL INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. I-TECH LAFACOS.

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BPOM Registered
Risk Class Kelas Resiko : B
LINEARZ Focused Ultrasound Stimulator System
Analysis ID: AKL 21603324416

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. I-TECH LAFACOS

AR Address

Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih

Registration Date

Jul 10, 2023

Expiry Date

Jan 20, 2026

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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