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Boditech RF IgM Control - Indonesia BPOM Medical Device Registration

Boditech RF IgM Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324127. The device is manufactured by BODITECH WITH INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ZOE PELITA NUSANTARA.

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
Boditech RF IgM Control
Analysis ID: AKL 20101324127

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BODITECH WITH INC.

Country of Origin

Korea

Authorized Representative

ZOE PELITA NUSANTARA

AR Address

JALAN CIKINI II NO 8 B

Registration Date

Oct 19, 2023

Expiry Date

Oct 01, 2027

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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