FUJI DRI-CHEM MIXING CUPS S - Indonesia BPOM Medical Device Registration

FUJI DRI-CHEM MIXING CUPS S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203320324. The device is manufactured by YUWA CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FUJIFILM INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : A

FUJI DRI-CHEM MIXING CUPS S

Analysis ID: AKL 10203320324

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

Country of Origin

Japan

Authorized Representative

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

Dec 04, 2023

Expiry Date

Jun 30, 2027

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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Other Products from YUWA CO., LTD.

Products from the same manufacturer (1 products)

FUJI DRI-CHEM Mixing Cups

Kelas Resiko : A

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Products with the same authorized representative (10 products)

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FUJI DRI-CHEM NX600i and Accessories

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Kelas Resiko : B

FUJI DRI-CHEM NX600 and Accessories

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Kelas Resiko : B

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Kelas Resiko : B

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Kelas Resiko : C

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Kelas Resiko : B

FUJI DRI-CHEM SLIDE LIP - P

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Kelas Resiko : B

FUJI DRI-CHEM Slide HDL-C-PIII D

FUJIFILM HEALTHCARE MANUFACTURING CORPORATION MINAMIASHIGARA NAKANUMA OFFICE.

Kelas Resiko : B