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LEICA ASP 300S Automated Vacuum Tissue Processor - Indonesia BPOM Medical Device Registration

LEICA ASP 300S Automated Vacuum Tissue Processor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203013984. The device is manufactured by LEICA BIOSYSTEMS NUSSLOCH GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.

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BPOM Registered
Risk Class Kelas Resiko : A
LEICA ASP 300S Automated Vacuum Tissue Processor
Analysis ID: AKL 10203013984

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

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

Pathology Equipment and Accessories

Tissue processing equipment (electrically operated)

Invitro Diagnostics

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DJ Fang

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