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LOFLO Line Cannula - Indonesia BPOM Medical Device Registration

LOFLO Line Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403025189. The device is manufactured by JAVID DE MEXICO S DE RL DE CV (WESTMED) from Mexico, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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 : A
LOFLO Line Cannula
Analysis ID: AKL 10403025189

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Mexico

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

Oct 12, 2020

Expiry Date

Aug 01, 2024

Product Type

Therapeutic Anesthesia Equipment

Nasal oxygen cannula.

Non Electromedic Non Sterile

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