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VENTANA HE 600 Systems and Accessories - Indonesia BPOM Medical Device Registration

VENTANA HE 600 Systems and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20203023590. The device is manufactured by Ventana Medical Systems Inc. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ROCHE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
VENTANA HE 600 Systems and Accessories
Analysis ID: AKL 20203023590

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Apr 03, 2023

Expiry Date

Jan 27, 2025

Product Type

Pathology Equipment and Accessories

Automated slide stainer.

Invitro Diagnostics

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