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NESCO Clinical Centrifuge - Indonesia BPOM Medical Device Registration

NESCO Clinical Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102127122. The device is manufactured by DLAB SCIENTIFIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.

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 : B
NESCO Clinical Centrifuge
Analysis ID: AKL 20102127122

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO. 26

Registration Date

Nov 19, 2021

Expiry Date

Nov 18, 2024

Product Type

Clinical Laboratory Equipment

Centrifugal chemistry analyzer for clinical use

Invitro Diagnostics

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