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ZYTOFAST PLUSH CISH Implementation Kit HRP-DAB - Indonesia BPOM Medical Device Registration

ZYTOFAST PLUSH CISH Implementation Kit HRP-DAB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20201917647. The device is manufactured by ZYTOVISION GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOZATIX 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
ZYTOFAST PLUSH CISH Implementation Kit HRP-DAB
Analysis ID: AKL 20201917647

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ZYTOVISION GMBH

Country of Origin

Germany

Authorized Representative

PT. BIOZATIX INDONESIA

AR Address

Jl. Griya Agung No.59 RT 02 RW 020

Registration Date

Jul 26, 2022

Expiry Date

Jun 30, 2025

Product Type

Biological Dyes

Immunohistochemistry reagents and kits (Quantitative).

Invitro Diagnostics

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