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AHFIL Glassionomer - Indonesia BPOM Medical Device Registration

AHFIL Glassionomer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602810223. The device is manufactured by ADVANCED HEALTHCARE LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KIANG MULTI CORPORATION.

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
AHFIL Glassionomer
Analysis ID: AKL 20602810223

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. KIANG MULTI CORPORATION

AR Address

Jl. Kyai Tapa No.5 AB R_t/w: 008/009 Kel. Tomang Kec. Grogol Petamburan Jakarta Barat - 11440

Registration Date

Sep 13, 2019

Expiry Date

Jan 31, 2024

Product Type

Prosthetic Dental Equipment

Dental cement.

Non Electromedic Non Sterile

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