myClip 2.0 Sectional Matrix Systems - Indonesia BPOM Medical Device Registration
myClip 2.0 Sectional Matrix Systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603027324. 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. TRI ANUGERAH JAYA.
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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
POLYDENTIA SACountry of Origin
Switzerland
Authorized Representative
PT. TRI ANUGERAH JAYAAR Address
Jl. Raya Pos Pengumben 34 G, RT/RW 002/005
Registration Date
Nov 29, 2020
Expiry Date
Jul 30, 2025
Product Type
Surgical Dental Equipment
Dental hand instrument.
Non Electromedic Non Sterile
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