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SANSIN A.V. Fistula Needle Sets - Indonesia BPOM Medical Device Registration

SANSIN A.V. Fistula Needle Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220537. The device is manufactured by JIANGXI SANXIN MEDTEC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : C
SANSIN A.V. Fistula Needle Sets
Analysis ID: AKL 20805220537

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Dec 28, 2022

Expiry Date

Oct 14, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Blood access device and accessories.

Non Electromedic Sterile

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