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HemaSpin TB-12 - Indonesia BPOM Medical Device Registration

HemaSpin TB-12 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209121162. The device is manufactured by DLAB SCIENTIFIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.

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
HemaSpin TB-12
Analysis ID: AKL 10209121162

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

- Ruko Bidex Blok G No. 30-31 Komplek CBD โ€“ BSD City Tangerang 15321 - Pergudangan Tekno Blok G3 No. 26 BSD City, Tangerang

Registration Date

Mar 17, 2021

Expiry Date

Mar 03, 2024

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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