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EndoActivator - Indonesia BPOM Medical Device Registration

EndoActivator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603026675. The device is manufactured by TIANJIN GOLDEN VENDOR TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DENTSPLY SIRONA 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
EndoActivator
Analysis ID: AKL 20603026675

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

DENTSPLY SIRONA INDONESIA

AR Address

Tempo Scan Tower 28th Floor, Jl. HR. Rasuna Said Kav.3-4 Kel. Kuningan Timur Kec. Setia Budi, Jakarta Selatan 12950

Registration Date

Nov 06, 2020

Expiry Date

May 07, 2024

Product Type

Surgical Dental Equipment

Dental handpiece and accessories

Non Radiation Electromedics

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