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SANKRINA Hollow Fiber Dialyzer (P Series) - Indonesia BPOM Medical Device Registration

SANKRINA Hollow Fiber Dialyzer (P Series) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805020922. The device is manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KARYATAMA MANDIRI BUSINESS.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
SANKRINA Hollow Fiber Dialyzer (P Series)
Analysis ID: AKL 20805020922

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. KARYATAMA MANDIRI BUSINESS

AR Address

Komplek Ruko D\'Best Blok B No. 39 Jl. RS Fatmawati No. 15 Gandaria Selatan

Registration Date

Aug 03, 2023

Expiry Date

May 24, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

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