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ZENTECH Extraction Buffer - Indonesia BPOM Medical Device Registration

ZENTECH Extraction Buffer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204911708. The device is manufactured by ZENTECH S.A from Belgium, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

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
ZENTECH Extraction Buffer
Analysis ID: AKL 10204911708

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ZENTECH S.A

Country of Origin

Belgium

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

Nov 26, 2021

Expiry Date

Jul 02, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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