D'LIV Derma Needling System - Indonesia BPOM Medical Device Registration
D'LIV Derma Needling System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421748. The device is manufactured by JEISYS MEDICAL INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is I-TECH LAFACOS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JEISYS MEDICAL INC.Country of Origin
Korea
Authorized Representative
I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Aug 07, 2024
Expiry Date
Apr 30, 2027
Product Type
Surgical Equipment
Microneedling Device for Aesthetic Use
Non Radiation Electromedics
