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KDL Urinal Bag - Indonesia BPOM Medical Device Registration

KDL Urinal Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320750. The device is manufactured by SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD, CHINA from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CITRA PERSADA MEDICINDO.

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
KDL Urinal Bag
Analysis ID: AKL 20805320750

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

CITRA PERSADA MEDICINDO

AR Address

Jl. DR. Ratulangi No. 7 B-1 Makassar Sulawesi Selatan

Registration Date

May 29, 2023

Expiry Date

Mar 01, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urine collector and accessories.

Non Electromedic Sterile

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