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DLAB DM0412 Clinical Centrifuge - Indonesia BPOM Medical Device Registration

DLAB DM0412 Clinical Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209719331. The device is manufactured by DLAB SCIENTIFIC, CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INTISUMBER HASILSEMPURNA.

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 : C
DLAB DM0412 Clinical Centrifuge
Analysis ID: AKL 20209719331

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INTISUMBER HASILSEMPURNA

AR Address

KOMPLEK DARMO PARK II BLOK IV NO. 14-15 JL. MAYJEND SUNGKONO SURABAYA

Registration Date

Mar 30, 2022

Expiry Date

Oct 01, 2025

Product Type

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

Automated cell-washing centrifuge for immuno-hematology.

Invitro Diagnostics

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DJ Fang

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