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DIROS OWL UNIVERSAL RF SYSTEM - Indonesia BPOM Medical Device Registration

DIROS OWL UNIVERSAL RF SYSTEM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002714446. The device is manufactured by DIROS TECHNOLOGY INC. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCHMIDT BIOMEDTECH INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
DIROS OWL UNIVERSAL RF SYSTEM
Analysis ID: AKL 21002714446

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Canada

Authorized Representative

PT. SCHMIDT BIOMEDTECH INDONESIA

AR Address

Gading Riverview Blok H-52 Jl. Mall of Indonesia Gate

Registration Date

Apr 27, 2022

Expiry Date

Dec 31, 2023

Product Type

Surgical Neurology Equipment

Radiofrequency lesion probe.

Non Radiation Electromedics

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