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VENTANA Antibody Diluent with Casein - Indonesia BPOM Medical Device Registration

VENTANA Antibody Diluent with Casein is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320528. 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 ROCHE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
VENTANA Antibody Diluent with Casein
Analysis ID: AKL 10204320528

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

ROCHE INDONESIA

AR Address

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

Registration Date

Jul 17, 2023

Expiry Date

May 16, 2028

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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