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B&E Calibration Pack For Electrolyte Analyzer - Indonesia BPOM Medical Device Registration

B&E Calibration Pack For Electrolyte Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421862. The device is manufactured by B&E BIO-TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is WHIRA PITOE JOINT VENTURE.

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BPOM Registered
Risk Class Kelas Resiko : B
B&E Calibration Pack For Electrolyte Analyzer
Analysis ID: AKL 20101421862

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

WHIRA PITOE JOINT VENTURE

AR Address

RUKO BUARAN PERSADA NO. 10, JL. JEND.POL.SOEKAMTO RT.008/06,KEL.DUREN SAWIT

Registration Date

Sep 24, 2024

Expiry Date

May 12, 2027

Product Type

Clinical Chemistry Test System

Calibrator (cair)

Invitro Diagnostics

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