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SIFARY Ultrasonic Endo Activation - Indonesia BPOM Medical Device Registration

SIFARY Ultrasonic Endo Activation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603027366. The device is manufactured by CHANGZHOU SIFARY MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REVO MEDIKA PARAHYANGAN.

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
SIFARY Ultrasonic Endo Activation
Analysis ID: AKL 20603027366

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. REVO MEDIKA PARAHYANGAN

AR Address

Jl Batununggal No. B5

Registration Date

Nov 29, 2020

Expiry Date

Jun 02, 2025

Product Type

Surgical Dental Equipment

Dental handpiece and accessories

Non Radiation Electromedics

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