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AUTOCHECK Lancing Device - Indonesia BPOM Medical Device Registration

AUTOCHECK Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603912630. The device is manufactured by MEDIFUN CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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
AUTOCHECK Lancing Device
Analysis ID: AKL 11603912630

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Taiwan (China)

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Feb 22, 2022

Expiry Date

Feb 22, 2025

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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