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MEGAPULSE HF Fraxx High Frequency Electro Surgical Unit - Indonesia BPOM Medical Device Registration

MEGAPULSE HF Fraxx High Frequency Electro Surgical Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603813223. The device is manufactured by LOKTAL MEDICAL ELECTRONICS INDUSTRIA E COMERCIO LTDA-EPP from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GLOBAL JAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : C
MEGAPULSE HF Fraxx High Frequency Electro Surgical Unit
Analysis ID: AKL 21603813223

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. GLOBAL JAYA MEDIKA

AR Address

Gedung Bersaudara Group Lantai 3A Lot.001 & 005 Jl. Penjernihan I No.38, Kelurahan Bendungan Hilir, Kecamatan Tanah Abang, Jakarta Pusat

Registration Date

May 05, 2023

Expiry Date

Apr 05, 2026

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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