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KERR PREMISA - Indonesia BPOM Medical Device Registration

KERR PREMISA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602815748. The device is manufactured by KERR CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PURE NOBLE SUN.

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BPOM Registered
Risk Class Kelas Resiko : B
KERR PREMISA
Analysis ID: AKL 20602815748

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

KERR CORPORATION.

Country of Origin

United States

Authorized Representative

PT. PURE NOBLE SUN

AR Address

Jl. Pecenongan No. 82 C Kebon Kelapa, Kec. Gambir Jakarta Pusat 10120

Registration Date

Mar 15, 2022

Expiry Date

Jul 29, 2024

Product Type

Prosthetic Dental Equipment

Tooth shade resin material.

Non Electromedic Non Sterile

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