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MEDNOVA Single Use Balloon Dilatation Catheters - Indonesia BPOM Medical Device Registration

MEDNOVA Single Use Balloon Dilatation Catheters is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501520051. The device is manufactured by ZHEJIANG CHUANGXIANG MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EDISON AMBASSADOR MEANS.

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
MEDNOVA Single Use Balloon Dilatation Catheters
Analysis ID: AKL 20501520051

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

EDISON AMBASSADOR MEANS

AR Address

Jl. Oasis Sememi Raya No. 1 RT 05 RW 04, Kel. Sememi, Kec. Benowo, Surabaya, Jawa Timur

Registration Date

Feb 06, 2025

Expiry Date

Jul 23, 2028

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

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