Tetric® N-Ceram 2 - Indonesia BPOM Medical Device Registration
Tetric® N-Ceram 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420394. The device is manufactured by IVOCLAR VIVADENT AG from Liechtenstein, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MURSMEDIC.
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 : 2
Manufacturer
IVOCLAR VIVADENT AGCountry of Origin
Liechtenstein
Authorized Representative
MURSMEDICAR Address
The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240
Registration Date
Oct 07, 2024
Expiry Date
Jul 31, 2026
Product Type
Prosthetic Dental Equipment
Tooth shade resin material.
Non Electromedic Non Sterile
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Tetric® N-PowerFlow 2
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