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RENAFILTER DIALYZER - Indonesia BPOM Medical Device Registration

RENAFILTER DIALYZER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420390. The device is manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. AESCOMED HEALTHCARE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
RENAFILTER DIALYZER
Analysis ID: AKL 20805420390

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

PT. AESCOMED HEALTHCARE INDONESIA

AR Address

GEDUNG OFFICE CITADEL BLOK F & G LANTAI 5, JL. DEWI SARTIKA NO. 3 Desa/Kelurahan Cililitan, Kec. Kramatjati, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta

Registration Date

Aug 01, 2024

Expiry Date

Jul 31, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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