Pure Global

BT SEDI 20 Auto ESR Analyzer - Indonesia BPOM Medical Device Registration

BT SEDI 20 Auto ESR Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206918207. The device is manufactured by SCIENTIFIC MEDICAL PRODUCTS SUN. SAN. AND TIC.LTD. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALIZAH.

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
BT SEDI 20 Auto ESR Analyzer
Analysis ID: AKL 20206918207

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. ALIZAH

AR Address

JL. OTISTA III NO.10A RT 001 RW 004 KEL.CIPINANG CEMPEDAK KEC.JATINEGARA

Registration Date

Dec 09, 2019

Expiry Date

Aug 02, 2024

Product Type

Manual Hematology Equipment

Erythrocyte sedimentation rate test (other, electrically operated)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing