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

WEGO A.V Fistula Needle Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805126398. The device is manufactured by SHANDONG WEIGAO BLOOD PURIFICATION PRODUCTS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. IMEDITECH SOLUTIONS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
WEGO A.V Fistula Needle Sets
Analysis ID: AKL 20805126398

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. IMEDITECH SOLUTIONS INDONESIA

AR Address

Menara Palma 12th Floor, Jalan H.R Rasuna Said Kaveling 6 Blok X-2, Unit 1233 dan 1234

Registration Date

Oct 28, 2021

Expiry Date

Dec 31, 2024

Product Type

Therapeutic Gastroenterology-Urology Equipment

Blood access device and accessories.

Non Electromedic Sterile

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