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KDL-INT NC RX PTCA Balloon Catheter - Indonesia BPOM Medical Device Registration

KDL-INT NC RX PTCA Balloon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505320240. The device is manufactured by SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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 : D
KDL-INT NC RX PTCA Balloon Catheter
Analysis ID: AKL 30505320240

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Jul 10, 2023

Expiry Date

Sep 06, 2025

Product Type

Therapeutic Cardiology Equipment

(Tidak digunakan) Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter (double)

Non Radiation Electromedics

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