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BM Test HbA1c Calibrator (1 dan 2) - Indonesia BPOM Medical Device Registration

BM Test HbA1c Calibrator (1 dan 2) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207110397. The device is manufactured by SEKISUI MEDICAL CO. LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SYSMEX 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.

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BPOM Registered
Risk Class Kelas Resiko : B
BM Test HbA1c Calibrator (1 dan 2)
Analysis ID: AKL 20207110397

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. SYSMEX INDONESIA

AR Address

Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13

Registration Date

Oct 21, 2024

Expiry Date

Feb 09, 2028

Product Type

Hematological Reagents

Calibrator for hemoglobin or hematocrit measurement.

Invitro Diagnostics

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