Pure Global

iPRO - Indonesia BPOM Medical Device Registration

iPRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203915725. The device is manufactured by BIOSYSTEMS, S.A from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FLEXYLABS INSTRUMENT 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
iPRO
Analysis ID: AKL 10203915725

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

BIOSYSTEMS, S.A

Country of Origin

Spain

Authorized Representative

PT. FLEXYLABS INSTRUMENT INDONESIA

AR Address

Ruko Poris Garden Blok A9A No.1A

Registration Date

Jan 25, 2023

Expiry Date

Dec 02, 2027

Product Type

Pathology Equipment and Accessories

Tissue processing equipment (electrically operated)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing