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HOB BioLINE Allergy Reagent Kit FD-1 - Indonesia BPOM Medical Device Registration

HOB BioLINE Allergy Reagent Kit FD-1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420339. The device is manufactured by HOB BIOTECH GROUP CORP., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOLAB UTAMA.

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
HOB BioLINE Allergy Reagent Kit FD-1
Analysis ID: AKL 20305420339

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INDOLAB UTAMA

AR Address

Rukan Mutiara Taman Palem E3 No. 9, Kel. Cengkareng Timur, Kec. Cengkareng, Jakarta Barat 11730

Registration Date

Jul 29, 2024

Expiry Date

Nov 13, 2028

Product Type

Immunological Test System

Immunoglobulins A, G, M, D, and E immunological test system.

Invitro Diagnostics

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