IPS Empress CAD - Indonesia BPOM Medical Device Registration

IPS Empress CAD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605911900. 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.

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BPOM Registered

Risk Class Kelas Resiko : B

IPS Empress CAD

Analysis ID: AKL 20605911900

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

Dec 05, 2021

Expiry Date

Jul 31, 2026

Product Type

Other Dental Equipment

Porcelain powder for clinical use.

Non Electromedic Non Sterile

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