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DIESTRO ISE Urine Diluent - Indonesia BPOM Medical Device Registration

DIESTRO ISE Urine Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204912000. The device is manufactured by JS MEDICINA ELECTRONICA S.R.L from Argentina, and is classified as Risk Class Kelas Resiko : A. 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 : A
DIESTRO ISE Urine Diluent
Analysis ID: AKL 10204912000

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Argentina

Authorized Representative

MULTISERA INDOSA

AR Address

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

Registration Date

Apr 03, 2023

Expiry Date

Jan 12, 2028

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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