Pure Global

GC DRY MOUTH GEL - Indonesia BPOM Medical Device Registration

GC DRY MOUTH GEL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605320639. The device is manufactured by GC CORPORATION FUJI OYAMA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHARMINDO LESTARI AWARD.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
GC DRY MOUTH GEL
Analysis ID: AKL 20605320639

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PHARMINDO LESTARI AWARD

AR Address

Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara, DKI Jakarta

Registration Date

Jun 07, 2023

Expiry Date

Oct 14, 2026

Product Type

Other Dental Equipment

Artificial saliva

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing