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JMS Plasma Extractor - Indonesia BPOM Medical Device Registration

JMS Plasma Extractor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209719603. The device is manufactured by W-ESPR TECHNOLOGY. CO. LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is KARINDO ALKESTRON.

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
JMS Plasma Extractor
Analysis ID: AKL 20209719603

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Feb 08, 2021

Expiry Date

Sep 17, 2025

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Automated blood cell separator

Invitro Diagnostics

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