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VITRO SARS-CoV-2 RT-PCR - Indonesia BPOM Medical Device Registration

VITRO SARS-CoV-2 RT-PCR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025702. The device is manufactured by VITRO S.A. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GRAHA MEGATAMA 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
VITRO SARS-CoV-2 RT-PCR
Analysis ID: AKL 20303025702

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VITRO S.A.

Country of Origin

Spain

Authorized Representative

GRAHA MEGATAMA INDONESIA

AR Address

RUKO MAHKOTA ANCOL BLOK. E 39 JL. BUDI MULIA KEL. PADEMANGAN BARAT

Registration Date

Sep 20, 2021

Expiry Date

Mar 27, 2025

Product Type

Serological Reagents

Respiratory viral panel multiplex nucleic acid assay

Invitro Diagnostics

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