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VITA AKZENT Plus Powders - Indonesia BPOM Medical Device Registration

VITA AKZENT Plus Powders is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20605810278. The device is manufactured by VITA ZAHNFABRIK H. RAUTER GMBH & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FONDACO JAYATAMA.

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
VITA AKZENT Plus Powders
Analysis ID: AKL 20605810278

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. FONDACO JAYATAMA

AR Address

APL Tower Podomoro City Lantai 27 T1, T2, T5, Jln Letjen S. Parman Kavling 28

Registration Date

Jan 02, 2025

Expiry Date

Oct 15, 2028

Product Type

Other Dental Equipment

Porcelain powder for clinical use.

Non Electromedic Non Sterile

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