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PD Foley Balloon Catheter - Indonesia BPOM Medical Device Registration

PD Foley Balloon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805900118. The device is manufactured by HOSPITAL EQUIPMENT MANUFACTURING COMPANY from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY.

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 : C
PD Foley Balloon Catheter
Analysis ID: AKL 20805900118

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

AR Address

Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560

Registration Date

May 05, 2023

Expiry Date

May 04, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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