ENVISION™ FLEX Antibody Diluent - Indonesia BPOM Medical Device Registration
ENVISION™ FLEX Antibody Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208817609. The device is manufactured by DAKO DENMARK APS. from Denmark, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DAKO DENMARK APS.Country of Origin
Denmark
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5
Registration Date
Aug 16, 2020
Expiry Date
May 22, 2024
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
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