DBS Laminate - Indonesia BPOM Medical Device Registration
DBS Laminate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201420048. The device is manufactured by DIAGNOSTIC BIOSYSTEMS from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FLEXYLABS INSTRUMENT INDONESIA.
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DBS Laminin
Risk Classification
Product Class
Kelas : 1
Manufacturer
DIAGNOSTIC BIOSYSTEMSCountry of Origin
United States
Authorized Representative
PT. FLEXYLABS INSTRUMENT INDONESIAAR Address
Ruko Poris Garden Blok A9A No.1A
Registration Date
Mar 15, 2024
Expiry Date
Feb 22, 2028
Product Type
Biological Dyes
Immunohistochemistry reagents and kits (Qualitative).
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