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FLEXO ST30 - Indonesia BPOM Medical Device Registration

FLEXO ST30 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403028004. The device is manufactured by CURATIVE MEDICAL TECHNOLOGY INC from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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 : C
FLEXO ST30
Analysis ID: AKL 20403028004

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Dec 18, 2020

Expiry Date

Mar 30, 2025

Product Type

Therapeutic Anesthesia Equipment

Positive airway pressure delivery system

Non Radiation Electromedics

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