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FRESENIUS Dialysis Fistula Needle - Indonesia BPOM Medical Device Registration

FRESENIUS Dialysis Fistula Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805904111. The device is manufactured by NIPRO CORPORATION LTD from Thailand, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS MEDICAL CARE INDONESIA.

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
FRESENIUS Dialysis Fistula Needle
Analysis ID: AKL 20805904111

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Thailand

Authorized Representative

PT. FRESENIUS MEDICAL CARE INDONESIA

AR Address

Tempo Scan Tower Lt.20 JL. HR Rasuna Said Kav 3-4, Kuningan , Jakarta Selatan

Registration Date

Jul 21, 2020

Expiry Date

Sep 19, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Blood access device and accessories.

Non Electromedic Sterile

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