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UNIDI Diluent (Model:DL) - Indonesia BPOM Medical Device Registration

UNIDI Diluent (Model:DL) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420123. The device is manufactured by HRJ BIOTECH MEDICAL CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRACIA VISI PRATAMA.

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
UNIDI Diluent (Model:DL)
Analysis ID: AKL 20208420123

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GRACIA VISI PRATAMA

AR Address

Jl. Soekarno Hatta No. 8A, Kel. Tlogosari Kulon, Kec. Pedurungan, Kota Semarang

Registration Date

Jul 08, 2024

Expiry Date

Jun 13, 2027

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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