LumiraDx INR Quality Control - Indonesia BPOM Medical Device Registration
LumiraDx INR Quality Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220302. The device is manufactured by HART BIOLOGICAL LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDQUEST GLOBAL PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HART BIOLOGICAL LTDCountry of Origin
United Kingdom
Authorized Representative
MEDQUEST GLOBAL PARTNERSAR Address
MENARA SALEMBA LANTAI 7, JALAN SALEMBA RAYA NOMOR 5-5A
Registration Date
Jun 06, 2023
Expiry Date
Jan 01, 2028
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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