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FUJIFILM SILVAMP Reader - Indonesia BPOM Medical Device Registration

FUJIFILM SILVAMP Reader is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102320525. The device is manufactured by NIDEC COPAL CORPORATION KORIYAMA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FUJIFILM INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
FUJIFILM SILVAMP Reader
Analysis ID: AKL 20102320525

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. FUJIFILM INDONESIA

AR Address

: EightyEight@Kasablanka Office Tower A, Lantai 36 Jl. Casablanca Raya Kav. 88, Desa/Kelurahan Menteng Dalam, Kec. Tebet, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12870 No Telp: 021-21282182

Registration Date

May 23, 2023

Expiry Date

Dec 09, 2027

Product Type

Clinical Laboratory Equipment

Instrumentation for clinical multiplex test systems.

Invitro Diagnostics

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