Pure Global

KANGJIN Collection Bag for Single Use - Indonesia BPOM Medical Device Registration

KANGJIN Collection Bag for Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805420439. The device is manufactured by JIANGSU KANGJIN MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SCINTILLATING ASIAN CENTER.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
KANGJIN Collection Bag for Single Use
Analysis ID: AKL 10805420439

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

SCINTILLATING ASIAN CENTER

AR Address

JL. PANTAI INDAH BARAT, KOMPLEK TOHO PANTAI INDAH KAPUK BLOK H NO. 25 & 27, Prov. DKI JAKARTA, KOTA JAKARTA UTARA, Kec. PENJARINGAN, Kel. KAMAL MUARA

Registration Date

Sep 05, 2024

Expiry Date

Feb 23, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urine collector and accessories

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing