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GALEMED Flextube - Indonesia BPOM Medical Device Registration

GALEMED Flextube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403918305. The device is manufactured by GALEMED (XIAMEN) CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MITRAPRIMA LESTARI.

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
GALEMED Flextube
Analysis ID: AKL 20403918305

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MITRAPRIMA LESTARI

AR Address

Rukan Sedayu Square Blok I No. 15, RT/RW 002/012, Kelurahan Cengkareng Barat

Registration Date

Dec 06, 2019

Expiry Date

Sep 30, 2024

Product Type

Therapeutic Anesthesia Equipment

Ventilator tubing.

Non Electromedic Non Sterile

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