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KUBOTA BenchTop Centrifuge - Indonesia BPOM Medical Device Registration

KUBOTA BenchTop Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209220002. The device is manufactured by KUBOTA MANUFACTURING CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DEMKA SAKTI.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
KUBOTA BenchTop Centrifuge
Analysis ID: AKL 10209220002

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Jan 11, 2022

Expiry Date

Aug 27, 2026

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Blood bank centrifuge for in vitro diagnostic use.

Invitro Diagnostics

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