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DAPI I Counterstain 2x500 µl (1000 ng/mL) - Indonesia BPOM Medical Device Registration

DAPI I Counterstain 2x500 µl (1000 ng/mL) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204023879. The device is manufactured by ABBOTT MOLECULAR INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SCIENCEWERKE.

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
DAPI I Counterstain 2x500 µl (1000 ng/mL)
Analysis ID: AKL 10204023879

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. SCIENCEWERKE

AR Address

Jl.Palmerah Barat No.25

Registration Date

May 30, 2024

Expiry Date

Dec 31, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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