JEISYS INTRAGen - Indonesia BPOM Medical Device Registration
JEISYS INTRAGen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603411861. The device is manufactured by JEISYS MEDICAL INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. I-TECH LAFACOS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JEISYS MEDICAL INC.Country of Origin
Korea
Authorized Representative
PT. I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Nov 17, 2022
Expiry Date
Oct 01, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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