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CURAWAY Disposable Biopsy Needle - Indonesia BPOM Medical Device Registration

CURAWAY Disposable Biopsy Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801520053. The device is manufactured by ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PURE SOUTHEAST ASIA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
CURAWAY Disposable Biopsy Needle
Analysis ID: AKL 20801520053

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PURE SOUTHEAST ASIA INDONESIA

AR Address

Equity Tower, 26th Floor H, Kav 52-53, Jl. Jenderal Sudirman

Registration Date

Feb 11, 2025

Expiry Date

Jun 25, 2029

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument

Non Electromedic Sterile

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