QIAGEN DML 3000 - Indonesia BPOM Medical Device Registration
QIAGEN DML 3000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102026414. The device is manufactured by PLEXUS MANUFACTURING SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
PLEXUS MANUFACTURING SDN. BHD.Country of Origin
Malaysia
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Apr 06, 2022
Expiry Date
Mar 21, 2026
Product Type
Clinical Laboratory Equipment
Colorimeter, photometer, or spectrophotometer for clinical use.
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