K1MED Aqua Injector - Indonesia BPOM Medical Device Registration
K1MED Aqua Injector is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902122359. The device is manufactured by K1MED CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BCS PRIMA INDONESIA.
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 : 2
Manufacturer
K1MED CO., LTDCountry of Origin
Korea
Authorized Representative
PT. BCS PRIMA INDONESIAAR Address
Jl. Pondok Kopi Raya Blok A No. 8 RT 009 RW 010
Registration Date
May 03, 2021
Expiry Date
Jan 21, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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