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A-Silicone for Bite Registration - Indonesia BPOM Medical Device Registration

A-Silicone for Bite Registration is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420039. The device is manufactured by SHANDONG HUGE DENTAL MATERIAL CORPORATION from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is QUALTEK CONSULTANT JAKARTA.

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
A-Silicone for Bite Registration
Analysis ID: AKL 20602420039

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Jan 29, 2024

Expiry Date

Oct 09, 2028

Product Type

Prosthetic Dental Equipment

Impression material.

Non Electromedic Non Sterile

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