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AiD™ HIV 1+2 Ag/Ab ELISA Plus - Indonesia BPOM Medical Device Registration

AiD™ HIV 1+2 Ag/Ab ELISA Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305911338. The device is manufactured by BEIJING WANTAI BIOLOGICAL PHARMACY ENTERPRISE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.

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 : D
AiD™ HIV 1+2 Ag/Ab ELISA Plus
Analysis ID: AKL 30305911338

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. SUMIFIN CITRA ABADI

AR Address

Ruko Banjar Wijaya Blok B1 No. 7 Kel. Poris Plawad Indah, Kec. Cipondoh, Tangerang, Banten

Registration Date

Aug 26, 2020

Expiry Date

Jul 01, 2025

Product Type

Immunological Test System

Multiple autoantibodies immunological test system.

Invitro Diagnostics

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