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MEDCAPTAIN Sample Diluent - Indonesia BPOM Medical Device Registration

MEDCAPTAIN Sample Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220001. The device is manufactured by MEDCAPTAIN MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 : B
MEDCAPTAIN Sample Diluent
Analysis ID: AKL 20208220001

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SABA INDOMEDIKA

AR Address

KOMP.KEDOYA ELOK PLAZA KAV DB/33 KEDOYA SELATAN

Registration Date

Jan 03, 2022

Expiry Date

Dec 31, 2024

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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