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POLYDENTIA Sectional Matrix Systems - Indonesia BPOM Medical Device Registration

POLYDENTIA Sectional Matrix Systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603420316. The device is manufactured by POLYDENTIA SA. from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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BPOM Registered
Risk Class Kelas Resiko : A
POLYDENTIA Sectional Matrix Systems
Analysis ID: AKL 10603420316

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

POLYDENTIA SA.

Country of Origin

Switzerland

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5

Registration Date

Oct 17, 2024

Expiry Date

May 31, 2029

Product Type

Surgical Dental Equipment

Dental hand instrument

Non Electromedic Non Sterile

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