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SYRAMED®µSP6000 Chroma X - Indonesia BPOM Medical Device Registration

SYRAMED®µSP6000 Chroma X is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221033. The device is manufactured by ARCOMED BY from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOSOPHA SAKTI.

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
SYRAMED®µSP6000 Chroma X
Analysis ID: AKL 20902221033

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ARCOMED BY

Country of Origin

Switzerland

Authorized Representative

PT. INDOSOPHA SAKTI

AR Address

Jl.Mampang Prapatan Raya No.1

Registration Date

Dec 23, 2022

Expiry Date

Feb 22, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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