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VENTANA HE 600 Differentiating Solution - Indonesia BPOM Medical Device Registration

VENTANA HE 600 Differentiating Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201613814. The device is manufactured by VENTANA MEDICAL SYSTEMS, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
VENTANA HE 600 Differentiating Solution
Analysis ID: AKL 10201613814

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. ROCHE INDONESIA

AR Address

Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi

Registration Date

May 01, 2020

Expiry Date

Jan 27, 2025

Product Type

Biological Dyes

Dye and chemical solution stains.

Invitro Diagnostics

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