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LMA Fastrach Single Use - Indonesia BPOM Medical Device Registration

LMA Fastrach Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403614475. The device is manufactured by PLAXTRON INDUSTRIAL (M) SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is IDS MEDICAL SYSTEMS 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
LMA Fastrach Single Use
Analysis ID: AKL 20403614475

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Oct 25, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Anesthesia Equipment

Tracheal tube.

Non Electromedic Sterile

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