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LEICA Cytovision for Karyotyping & FISH and Accessories - Indonesia BPOM Medical Device Registration

LEICA Cytovision for Karyotyping & FISH and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304028703. The device is manufactured by LEICA BIOSYSTEMS RICHMOND., INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.

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BPOM Registered
Risk Class Kelas Resiko : C
LEICA Cytovision for Karyotyping & FISH and Accessories
Analysis ID: AKL 20304028703

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BIOGEN SCIENTIFIC

AR Address

Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21

Registration Date

May 10, 2022

Expiry Date

Dec 31, 2023

Product Type

Immunology Laboratory Equipment and Reagents

Automated fluorescence in situ hybridization (FISH) enumeration systems

Invitro Diagnostics

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