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DRG Progesterone Elisa - Indonesia BPOM Medical Device Registration

DRG Progesterone Elisa is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101121882. The device is manufactured by DRG INSTRUMENTS GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOZATIX INDONESIA.

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
DRG Progesterone Elisa
Analysis ID: AKL 20101121882

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. BIOZATIX INDONESIA

AR Address

Jl. Griya Agung No.59 RT 02 RW 020

Registration Date

Mar 17, 2021

Expiry Date

Jun 24, 2025

Product Type

Clinical Chemistry Test System

Progesterone test system (kit & cair)

Invitro Diagnostics

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