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Cortisol ELISA - Indonesia BPOM Medical Device Registration

Cortisol ELISA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101915740. The device is manufactured by LABOR DIAGNOSTIKA NORD GMBH & CO. KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. Rafa Topaz Main.

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
Cortisol ELISA
Analysis ID: AKL 20101915740

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. Rafa Topaz Main

AR Address

Taman Buaran Indah I Blok U No. 242 Jl. Radin Inten II, Klender, Jakarta Timur

Registration Date

Sep 06, 2019

Expiry Date

Apr 01, 2024

Product Type

Clinical Chemistry Test System

Cortisol (hydrocortisone and hydroxycorticosterone) test system (kit & cair)

Invitro Diagnostics

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