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HAEMONECTICS Post-Process Filter System for Platelets - Indonesia BPOM Medical Device Registration

HAEMONECTICS Post-Process Filter System for Platelets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209716828. The device is manufactured by HAEMONECTICS MANUFACTURING INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRANSMEDIC 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
HAEMONECTICS Post-Process Filter System for Platelets
Analysis ID: AKL 20209716828

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137

Registration Date

Jun 02, 2021

Expiry Date

Aug 26, 2025

Product Type

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

Transfer set.

Invitro Diagnostics

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