EDAN BGE Control Level 3 - Indonesia BPOM Medical Device Registration
EDAN BGE Control Level 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420018. The device is manufactured by EDAN INSTRUMENT, INC., from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUSANTARA MEDCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EDAN INSTRUMENT, INC.,Country of Origin
China
Authorized Representative
PT. NUSANTARA MEDCARE INDONESIAAR Address
NUSANTARA MEDCARE INDONESIA
Registration Date
Jan 05, 2024
Expiry Date
Jul 31, 2027
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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