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RENMED AV FISTULA - Indonesia BPOM Medical Device Registration

RENMED AV FISTULA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320747. 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 AV FISTULA
Analysis ID: AKL 20805320747

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. RENALMED TIARA MAIN

AR Address

Gedung Enseval Lantai 2 Jl. Pulo Lentut No. 10 Kawasan Industri Pulogadung, Jakarta Timur Tlp. 021-4618330

Registration Date

May 25, 2023

Expiry Date

Mar 03, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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RENMED DIALYZER Low Flux L160

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Kelas Resiko : C

RENMED Hemodialysis Blood Tubing Set

SHANDONG WEIGAO BLOOD PURIFICATION PRODUCTS CO., LTD.

Kelas Resiko : C