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MENOX ™ Liquid Embolic System - Indonesia BPOM Medical Device Registration

MENOX ™ Liquid Embolic System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003023594. The device is manufactured by MERIL LIFE SCIENCES PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. WORCKHARDT PHARMA INDO.

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 : D
MENOX ™ Liquid Embolic System
Analysis ID: AKL 31003023594

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. WORCKHARDT PHARMA INDO

AR Address

Ruko Mega Grosir Blok P 16 Cempaka Mas JL.Letjen Suprapto ,Sumur Batu

Registration Date

Jun 30, 2020

Expiry Date

Aug 31, 2024

Product Type

Therapeutic Neurology Equipment

Neurovascular embolization device.

Non Electromedic Sterile

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