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MEDCAPTAIN Pre-Trigger Solution - Indonesia BPOM Medical Device Registration

MEDCAPTAIN Pre-Trigger Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204128110. The device is manufactured by MEDCAPTAIN MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SABA INDOMEDIKA.

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 : A
MEDCAPTAIN Pre-Trigger Solution
Analysis ID: AKL 10204128110

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

SABA INDOMEDIKA

AR Address

KOMP.KEDOYA ELOK PLAZA KAV DB/33 KEDOYA SELATAN

Registration Date

Dec 22, 2021

Expiry Date

Dec 31, 2024

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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