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SELF CURE ACTIVATOR - Indonesia BPOM Medical Device Registration

SELF CURE ACTIVATOR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602902698. The device is manufactured by DENTSPLY CAULK. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DENTSPLY SIRONA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
SELF CURE ACTIVATOR
Analysis ID: AKL 20602902698

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DENTSPLY CAULK.

Country of Origin

United States

Authorized Representative

PT. 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

Mar 10, 2023

Expiry Date

Apr 01, 2026

Product Type

Prosthetic Dental Equipment

Resin tooth bonding agent.

Non Electromedic Non Sterile

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