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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
GMMC.Country of Origin
Korea
Authorized Representative
MEDISINDO BAHANAAR 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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