Pure Global

SuperFlex Trigger Solution - Indonesia BPOM Medical Device Registration

SuperFlex Trigger Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420194. The device is manufactured by SUZHOU SYM-BIO LIFESCIENCE CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is DARMA LABORA 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
SuperFlex Trigger Solution
Analysis ID: AKL 10204420194

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

DARMA LABORA INDONESIA

AR Address

KAWASAN INDUSTRI JABABEKA 7, BLOK B3/B, DESA WANGUNHARJA

Registration Date

Aug 28, 2024

Expiry Date

Apr 24, 2029

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing