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BRIGHT Bond Universal - Indonesia BPOM Medical Device Registration

BRIGHT Bond Universal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602025397. The device is manufactured by GENOSS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ICT WORLDWIDE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
BRIGHT Bond Universal
Analysis ID: AKL 20602025397

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GENOSS CO., LTD

Country of Origin

Korea

Authorized Representative

ICT WORLDWIDE INDONESIA

AR Address

Office 88 Lantai 25 Unit H, Jl. Casablanca Raya Kav. 88

Registration Date

Sep 16, 2020

Expiry Date

Jul 20, 2025

Product Type

Prosthetic Dental Equipment

Resin tooth bonding agent.

Non Electromedic Non Sterile

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