SEFFILLER - Indonesia BPOM Medical Device Registration
SEFFILLER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603127650. The device is manufactured by SEFFILINE S.R.L from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHARMINDO RHIZOME STURDY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEFFILINE S.R.LCountry of Origin
Italy
Authorized Representative
PHARMINDO RHIZOME STURDYAR Address
Jalan Arowana No 98 Kel. Kebonagung Kec. Kaliwates
Registration Date
May 10, 2023
Expiry Date
Feb 27, 2026
Product Type
Surgical Equipment
Microneedling Device for Aesthetic Use
Non Electromedic Sterile

