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Z-5 Atrioseptostomy Catheter - Indonesia BPOM Medical Device Registration

Z-5 Atrioseptostomy Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501013992. The device is manufactured by NUMED CANADA, INC. from Canada, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NUGRA KARSERA.

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
Z-5 Atrioseptostomy Catheter
Analysis ID: AKL 20501013992

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

NUMED CANADA, INC.

Country of Origin

Canada

Authorized Representative

PT. NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Dec 15, 2022

Expiry Date

Dec 31, 2024

Product Type

Diagnostic Cardiology Equipment

Diagnostic intravascular catheter.

Non Electromedic Sterile

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