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VITIQUE Silane - Indonesia BPOM Medical Device Registration

VITIQUE Silane is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602512834. The device is manufactured by DMG CHEMISCH-PHARMAZEUTISCH FABRIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. THOMASONG NIRMALA.

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
VITIQUE Silane
Analysis ID: AKL 20602512834

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. THOMASONG NIRMALA

AR Address

JL. AM SANGAJI NO. 20A KEL. PETOJO UTARA, KEC. GAMBIR JAKARTA TELP. 021-63855888

Registration Date

Mar 28, 2019

Expiry Date

Feb 21, 2024

Product Type

Prosthetic Dental Equipment

Denture relining, repairing, or rebasing resin.

Non Electromedic Non Sterile

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