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Hilab Flow - Indonesia BPOM Medical Device Registration

Hilab Flow is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420113. The device is manufactured by HI TECHNOLOGIES LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is KIRANA JAYA LESTARI.

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
Hilab Flow
Analysis ID: AKL 20304420113

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

KIRANA JAYA LESTARI

AR Address

Jl. Tanah Abang II No. 37 RT.001/RW.003, Kode Pos 10160, Kel. Petojo Selatan, Kec. Gambir, Kota Jakarta Pusat, Provinsi DKI Jakarta

Registration Date

Dec 02, 2024

Expiry Date

Jan 23, 2029

Product Type

Immunology Laboratory Equipment and Reagents

Immunofluorometer equipment

Invitro Diagnostics

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