K2 Blood Tube Stripper - Indonesia BPOM Medical Device Registration
K2 Blood Tube Stripper is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203420201. The device is manufactured by W-ESPR TECHNOLOGY CO LTD from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
W-ESPR TECHNOLOGY CO LTDCountry of Origin
Taiwan (China)
Authorized Representative
PT. FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Dec 19, 2024
Expiry Date
Aug 12, 2028
Product Type
Pathology Equipment and Accessories
Device for sealing microsections. (Non Electrically Operated)
Non Electromedic Non Sterile
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