SUNWAY Vacuum Blood Collection System EDTA K3 Tube (PET) - Indonesia BPOM Medical Device Registration

SUNWAY Vacuum Blood Collection System EDTA K3 Tube (PET) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101917663. The device is manufactured by WEIHAI SUNWAY MEDICAL TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.

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BPOM Registered

Risk Class Kelas Resiko : B

SUNWAY Vacuum Blood Collection System EDTA K3 Tube (PET)

Analysis ID: AKL 20101917663

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

WEIHAI SUNWAY MEDICAL TECHNOLOGY CO.,LTD

Country of Origin

China

Authorized Representative

PT. MAIN MEDICAL CHAKRA

AR Address

FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon

Registration Date

Jul 18, 2023

Expiry Date

Jun 06, 2028

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

DJ Fang

MedTech Regulatory Expert

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SUNWAY Vacuum Blood Collection System Lithium Heparin Tube (PET)

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