Pure Global

PROTSMART™ 6 - Indonesia BPOM Medical Device Registration

PROTSMART™ 6 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209520028. The device is manufactured by MEDICA S.P.A from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MARTHA INTI PERSADA.

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 : C
PROTSMART™ 6
Analysis ID: AKL 20209520028

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDICA S.P.A

Country of Origin

Italy

Authorized Representative

MARTHA INTI PERSADA

AR Address

Ruko BIZHUB Blok RC No. 15, Jalan Raya Serpong 99

Registration Date

Jan 30, 2025

Expiry Date

Sep 05, 2029

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Empty container for the collection and processing of blood and blood components.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from MARTHA INTI PERSADA
Products with the same authorized representative (2 products)