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MI Pistor Eliance - Indonesia BPOM Medical Device Registration

MI Pistor Eliance is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420001. The device is manufactured by MI - MEDICAL INNOVATION from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REDO MARKETING 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
MI Pistor Eliance
Analysis ID: AKL 20902420001

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

France

Authorized Representative

PT. REDO MARKETING INDONESIA

AR Address

Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang

Registration Date

Jan 03, 2024

Expiry Date

Sep 15, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Radiation Electromedics

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