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Ci-Ca Dialysate K4 5000 mL - Indonesia BPOM Medical Device Registration

Ci-Ca Dialysate K4 5000 mL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805120219. The device is manufactured by FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH from Germany, 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
Ci-Ca Dialysate K4 5000 mL
Analysis ID: AKL 20805120219

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

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

Dec 22, 2022

Expiry Date

Sep 01, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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