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BLESSMED Transcutaneous Jaundice Detector - Indonesia BPOM Medical Device Registration

BLESSMED Transcutaneous Jaundice Detector is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501313585. The device is manufactured by XUZHOU KEJIAN HI-TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BLESINDO INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
BLESSMED Transcutaneous Jaundice Detector
Analysis ID: AKL 21501313585

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BLESINDO INDONESIA

AR Address

Ruko Duren Sawit Center No. 9B, Jl Duren Sawit Raya

Registration Date

Nov 26, 2020

Expiry Date

Nov 26, 2023

Product Type

Clinical Chemistry Test System

Bilirubin (total and unbound) in the neonate test system (strip & midstream)

Non Radiation Electromedics

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