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HEMO-CATH LT Silicone Double Catheter Set - Indonesia BPOM Medical Device Registration

HEMO-CATH LT Silicone Double Catheter Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805122392. The device is manufactured by MEDICAL COMPONENTS INC. DBA MEDCOMP from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SINAR MULIA INDOMEDIKA.

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
HEMO-CATH LT Silicone Double Catheter Set
Analysis ID: AKL 20805122392

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. SINAR MULIA INDOMEDIKA

AR Address

Ruko Premier Park 2 Block : AB No.26, Modernland Cikokol Tangerang

Registration Date

May 01, 2021

Expiry Date

Jun 30, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Blood access device and accessories.

Non Electromedic Sterile

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