Pure Global

Pearl NC: Post Dilation Catheter - Indonesia BPOM Medical Device Registration

Pearl NC: Post Dilation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321075. The device is manufactured by RELISYS MEDICAL DEVICES LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is AGRAPANA MULIA 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
Pearl NC: Post Dilation Catheter

Pearl NC: Post Dilatation Catheter

Analysis ID: AKL 20501321075

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

AGRAPANA MULIA MEDIKA

AR Address

ITC Cempaka Mas Mega Grosir Lantai 8 No 8A Jl. Letjend Suprapto Kav.1

Registration Date

Oct 14, 2023

Expiry Date

Jul 10, 2028

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from RELISYS MEDICAL DEVICES LTD
Products from the same manufacturer (2 products)