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RENMED Dialyzers LF16 - Indonesia BPOM Medical Device Registration

RENMED Dialyzers LF16 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420207. The device is manufactured by SHANDONG WEIGAO BLOOD PURIFICATION PRODUCTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RENALMED TIARA MAIN.

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
RENMED Dialyzers LF16
Analysis ID: AKL 20805420207

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. RENALMED TIARA MAIN

AR Address

JL.PULO LENTUT NO. 12, Lt.2 Unit 2B, KAWASAN INDUSTRI PULOGADUNG

Registration Date

Apr 29, 2024

Expiry Date

Apr 29, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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