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NESCO Multicheck 2 - Indonesia BPOM Medical Device Registration

NESCO Multicheck 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421346. The device is manufactured by BIOPTIK TECHNOLOGY INC from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.

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BPOM Registered
Risk Class Kelas Resiko : C
NESCO Multicheck 2
Analysis ID: AKL 20101421346

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO.26,JLR.E MARTADINATA ,Desa/Kelurahan Pademangan Barat, Kec.Pademangan,Kota Adm.Jakarta Utara, Provinsi DKI Jakarta. Kode Pos:14420

Registration Date

Jul 08, 2024

Expiry Date

Jul 08, 2027

Product Type

Clinical Chemistry Test System

Multi parameter clinical chemistry test system

Invitro Diagnostics

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