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MASTER-DENT Light Cure Cavity Liner - Indonesia BPOM Medical Device Registration

MASTER-DENT Light Cure Cavity Liner is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602520052. The device is manufactured by DENTONICS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRI ANUGERAH JAYA.

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BPOM Registered
Risk Class Kelas Resiko : C
MASTER-DENT Light Cure Cavity Liner
Analysis ID: AKL 20602520052

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

DENTONICS, INC.

Country of Origin

United States

Authorized Representative

TRI ANUGERAH JAYA

AR Address

Jl. Raya Pos Pengumben 34 G

Registration Date

Feb 10, 2025

Expiry Date

Nov 01, 2029

Product Type

Prosthetic Dental Equipment

Calcium hydroxide cavity liner.

Non Electromedic Non Sterile

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