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LIFOTRONIC AirPro-600 Air Compression Therapy System - Indonesia BPOM Medical Device Registration

LIFOTRONIC AirPro-600 Air Compression Therapy System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505220146. The device is manufactured by SHENZHEN LIFOTRONIC TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LIFOTRONIC TECHNOLOGY 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
LIFOTRONIC AirPro-600 Air Compression Therapy System
Analysis ID: AKL 20505220146

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. LIFOTRONIC TECHNOLOGY INDONESIA

AR Address

LIFOTRONIC TECHNOLOGY INDONESIA

Registration Date

Dec 26, 2022

Expiry Date

Oct 27, 2027

Product Type

Therapeutic Cardiology Equipment

Compressible limb sleeve.

Non Radiation Electromedics

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