xMAP Sheath Concentrate PLUS - Indonesia BPOM Medical Device Registration
xMAP Sheath Concentrate PLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204122414. The device is manufactured by LUMINEX CORPORATION from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is GENECRAFT LABS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LUMINEX CORPORATIONCountry of Origin
United States
Authorized Representative
GENECRAFT LABSAR Address
Business Park kebon Jeruk Blok F2 No 9 Jl. Meruya Ilir Raya No. 88
Registration Date
May 05, 2021
Expiry Date
Oct 20, 2025
Product Type
Reagents and Specimen Providers
General purpose reagent.
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