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BENQ Qflux Dialyzer - Indonesia BPOM Medical Device Registration

BENQ Qflux Dialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805126342. The device is manufactured by BENQ DIALYSIS TECHNOLOGY CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
BENQ Qflux Dialyzer
Analysis ID: AKL 20805126342

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

- Ruko Bidex Blok G No. 30-31 Komplek CBD โ€“ BSD City Tangerang 15321 - Pergudangan Tekno Blok G3 No. 26 BSD City, Tangerang

Registration Date

Oct 25, 2021

Expiry Date

Jul 27, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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