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DIESTRO-Trilevel Quality Control Solutions - Indonesia BPOM Medical Device Registration

DIESTRO-Trilevel Quality Control Solutions is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101912216. The device is manufactured by JS MEDICINA ELECTRONICA S.R.L. from Argentina, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTISERA INDOSA.

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
DIESTRO-Trilevel Quality Control Solutions
Analysis ID: AKL 20101912216

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Argentina

Authorized Representative

MULTISERA INDOSA

AR Address

JL. JEND. SUDIRMAN NO. 689 RT/RW : 21/07

Registration Date

Mar 31, 2023

Expiry Date

Jan 12, 2028

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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