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REMA Extracorporeal Blood Circuit of Blood Purification Equipment - Indonesia BPOM Medical Device Registration

REMA Extracorporeal Blood Circuit of Blood Purification Equipment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220240. The device is manufactured by WEGO HEALTHCARE (SHENZHEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SING AJI SENTOSA.

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BPOM Registered
Risk Class Kelas Resiko : C
REMA Extracorporeal Blood Circuit of Blood Purification Equipment
Analysis ID: AKL 20805220240

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SING AJI SENTOSA

AR Address

Jl. Raya Pondok Gede No. 3 Pinang Ranti, Makassar, Jakarta Timur

Registration Date

Aug 11, 2022

Expiry Date

Aug 08, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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