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JOKOH Standard Solution 2 - Indonesia BPOM Medical Device Registration

JOKOH Standard Solution 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101013121. The device is manufactured by JOKOH CORPORATION LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SUMBERMITRA AGUNGJAYA.

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
JOKOH Standard Solution 2
Analysis ID: AKL 20101013121

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

SUMBERMITRA AGUNGJAYA

AR Address

Gading Bukit Indah, Blok H/3 Kel Kelapa Gading Barat, Kec Kelapa Gading Jakarta Utara

Registration Date

Aug 04, 2023

Expiry Date

Jul 14, 2028

Product Type

Clinical Chemistry Test System

Calibrator (cair)

Invitro Diagnostics

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