LENOSOFT - Indonesia BPOM Medical Device Registration
LENOSOFT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902220665. The device is manufactured by FARMABAN, S.A. from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BETWEEN PARTNERS OF SELF-SUFFICIENCY.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FARMABAN, S.A.Country of Origin
Spain
Authorized Representative
BETWEEN PARTNERS OF SELF-SUFFICIENCYAR Address
Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560
Registration Date
Jul 04, 2022
Expiry Date
Apr 20, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
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