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FUJIFILM SILVAMP TB LAM II - Indonesia BPOM Medical Device Registration

FUJIFILM SILVAMP TB LAM II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20302320391. The device is manufactured by FUJIFILM YUWA MEDICAL PRODUCTS VIETNAM COMPANY LIMITED from Vietnam, 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 TB LAM II
Analysis ID: AKL 20302320391

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Vietnam

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

Nov 17, 2023

Expiry Date

Dec 09, 2027

Product Type

Microbiology Equipment

Microorganism differentiation and identification device.

Invitro Diagnostics

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