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FARCATH Double Lumen Haemodialysis Catheter Kit - Indonesia BPOM Medical Device Registration

FARCATH Double Lumen Haemodialysis Catheter Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805120151. The device is manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DIAN LANGGENG PRATAMA.

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BPOM Registered
Risk Class Kelas Resiko : C
FARCATH Double Lumen Haemodialysis Catheter Kit
Analysis ID: AKL 20805120151

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DIAN LANGGENG PRATAMA

AR Address

Jl. Raden Saleh Raya No. 4

Registration Date

Jan 08, 2021

Expiry Date

Jan 01, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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DJ Fang

DJ Fang

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