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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.

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BPOM Registered
Risk Class Kelas Resiko : B
K1MED Aqua Injector
Analysis ID: AKL 20902122359

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

K1MED CO., LTD

Country of Origin

Korea

Authorized Representative

PT. BCS PRIMA INDONESIA

AR 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.

Non Radiation Electromedics

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