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RENACARE AV Fistula Needle Sets - Indonesia BPOM Medical Device Registration

RENACARE AV Fistula Needle Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220392. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
RENACARE AV Fistula Needle Sets
Analysis ID: AKL 20805220392

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

Oct 27, 2022

Expiry Date

Jul 28, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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