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Vysis Paraffin Pretreatment IV & Post-Hybridization Wash Buffer Kit - Indonesia BPOM Medical Device Registration

Vysis Paraffin Pretreatment IV & Post-Hybridization Wash Buffer Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304022011. The device is manufactured by ABBOTT MOLECULAR INC. from United States, and is classified as Risk Class Kelas Resiko : C. 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 : C
Vysis Paraffin Pretreatment IV & Post-Hybridization Wash Buffer Kit
Analysis ID: AKL 20304022011

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. SCIENCEWERKE

AR Address

Jl.Palmerah Barat No.25

Registration Date

May 27, 2024

Expiry Date

Dec 31, 2026

Product Type

Immunology Laboratory Equipment and Reagents

Automated fluorescence in situ hybridization (FISH) enumeration systems

Invitro Diagnostics

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DJ Fang

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