Pure Global

HELMER PF96i Sharrer - Indonesia BPOM Medical Device Registration

HELMER PF96i Sharrer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205420017. The device is manufactured by HELMER INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRISMED HOSLAB 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
HELMER PF96i Sharrer

HELMER PF96i Agitator

Analysis ID: AKL 20205420017

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HELMER INC

Country of Origin

United States

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321

Registration Date

Jan 22, 2024

Expiry Date

Dec 31, 2025

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated platelet aggregation system.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing