IvoBase® Hybrid - Indonesia BPOM Medical Device Registration

IvoBase® Hybrid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602122533. 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 PT. 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.

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BPOM Registered

Risk Class Kelas Resiko : B

IvoBase® Hybrid

Analysis ID: AKL 20602122533

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

IVOCLAR VIVADENT AG

Country of Origin

Liechtenstein

Authorized Representative

AR Address

Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat

Registration Date

Aug 02, 2022

Expiry Date

Jul 31, 2026

Product Type

Prosthetic Dental Equipment

Denture relining, repairing, or rebasing resin.

Non Electromedic Non Sterile

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