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NIHON PER Reticulonac MK-110W - Indonesia BPOM Medical Device Registration

NIHON PER Reticulonac MK-110W is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201220378. The device is manufactured by NIHON KOHDEN TOMIOKA CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GANDASARI EKASATYA.

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Risk Class Kelas Resiko : A
NIHON PER Reticulonac MK-110W

NIHON KOHDEN Reticulonac MK-110W

Analysis ID: AKL 10201220378

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. GANDASARI EKASATYA

AR Address

Jl. Raya Mabes Hankam No.5 9A, RT.7/RW.2

Registration Date

Nov 11, 2024

Expiry Date

May 30, 2026

Product Type

Biological Dyes

Dye and chemical solution stains.

Invitro Diagnostics

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