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PURIFIER L120 Low Flow Dialyser - Indonesia BPOM Medical Device Registration

PURIFIER L120 Low Flow Dialyser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220095. The device is manufactured by SAFIL MEDICAL PRODUCTS INTERNATIONAL TRANSPORT INDUSTRY AND TRADE CO., LTD., from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is RENALMED TIARA MAIN.

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Risk Class Kelas Resiko : C
PURIFIER L120 Low Flow Dialyser

PURIFIER L120 Low Flux Dialyser

Analysis ID: AKL 20805220095

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

RENALMED TIARA MAIN

AR Address

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

Registration Date

Apr 08, 2022

Expiry Date

Jul 13, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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