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MYQUICKMAT Forte Starter Kit - Indonesia BPOM Medical Device Registration

MYQUICKMAT Forte Starter Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603420309. The device is manufactured by POLYDENTIA SA from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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 : A
MYQUICKMAT Forte Starter Kit
Analysis ID: AKL 10603420309

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

POLYDENTIA SA

Country of Origin

Switzerland

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5

Registration Date

Aug 21, 2024

Expiry Date

May 31, 2029

Product Type

Surgical Dental Equipment

Dental hand instrument

Non Electromedic Non Sterile

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