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SRI DIALYSIS POWDER B - Indonesia BPOM Medical Device Registration

SRI DIALYSIS POWDER B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220031. The device is manufactured by LIAONING TRUSTONG BIOLOGICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RENAL FACILITIES INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
SRI DIALYSIS POWDER B
Analysis ID: AKL 20805220031

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. RENAL FACILITIES INDONESIA

AR Address

Ruko Golden Boulevard Blok G 2/39 BSD City Kel. Lengkong Karya, Kec. Serpong Utara, Kota Tangerang Selatan

Registration Date

Feb 11, 2022

Expiry Date

Dec 30, 2023

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Non Sterile

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