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FUJI DRYPIX LITE Medical Dry Imager - Indonesia BPOM Medical Device Registration

FUJI DRYPIX LITE Medical Dry Imager is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501714432. The device is manufactured by FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD. from China, 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
FUJI DRYPIX LITE Medical Dry Imager
Analysis ID: AKL 21501714432

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

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

Mar 15, 2024

Expiry Date

Jun 30, 2028

Product Type

Diagnostic Radiology Equipment

Medical image digitizer.

Non Radiation Electromedics

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