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AGAPPE Dengue Combi - Indonesia BPOM Medical Device Registration

AGAPPE Dengue Combi is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420176. The device is manufactured by AGAPPE DIAGNOSTICS LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.

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 : C
AGAPPE Dengue Combi
Analysis ID: AKL 20303420176

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. MULTIMEDILAB KARYAMANDIRI

AR Address

GP plaza lantai 3 unit 6, jalan Gelora II No. 01

Registration Date

May 07, 2024

Expiry Date

Feb 07, 2027

Product Type

Serological Reagents

Dengue virus serological reagents

Invitro Diagnostics

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