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SHOFU GLASIONOMER FX ULTRA - Indonesia BPOM Medical Device Registration

SHOFU GLASIONOMER FX ULTRA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602818722. The device is manufactured by SHOFU, INC. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MORITA DENTAL INDO.

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
SHOFU GLASIONOMER FX ULTRA
Analysis ID: AKL 20602818722

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SHOFU, INC.

Country of Origin

Japan

Authorized Representative

MORITA DENTAL INDO

AR Address

Ruko Roxy Trade Center Jl. KH. Hasyim Ashari No.233 K Kel.Cideng Kec.Gambir

Registration Date

Feb 27, 2023

Expiry Date

Nov 29, 2027

Product Type

Prosthetic Dental Equipment

Tooth shade resin material.

Non Electromedic Sterile

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