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BRIGHT Impress Putty - Indonesia BPOM Medical Device Registration

BRIGHT Impress Putty is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602127079. 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.

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
BRIGHT Impress Putty
Analysis ID: AKL 20602127079

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

Nov 18, 2021

Expiry Date

Feb 18, 2026

Product Type

Prosthetic Dental Equipment

Impression material.

Non Electromedic Non Sterile

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