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ELIZER Guiding Catheter - Indonesia BPOM Medical Device Registration

ELIZER Guiding Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320981. The device is manufactured by DOLPHIN LIFE SCIENCE INDIA, LLP from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOMED PHARMA.

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
ELIZER Guiding Catheter
Analysis ID: AKL 20501320981

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. INDOMED PHARMA

AR Address

Kelapa Gading Hyper Mall, Lantai Dasar Blok B10 No. 03 (DB1003), Jakarta Utara

Registration Date

Nov 24, 2023

Expiry Date

Aug 14, 2025

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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