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FAMILY DR Lancing Device - Indonesia BPOM Medical Device Registration

FAMILY DR Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603719061. The device is manufactured by GMMC. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDISINDO BAHANA.

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
FAMILY DR Lancing Device
Analysis ID: AKL 11603719061

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

GMMC.

Country of Origin

Korea

Authorized Representative

MEDISINDO BAHANA

AR Address

Rukan Graha Cempaka Mas Blok E No.15 Lt.3, Jl. Letjen Suprapto No.1, Jakarta Pusat

Registration Date

Feb 24, 2022

Expiry Date

Jan 13, 2027

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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