MESOESTETIC® MESOHYAL™ DMAE - Indonesia BPOM Medical Device Registration
MESOESTETIC® MESOHYAL™ DMAE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602021578. The device is manufactured by MESOESTETIC PHARMA GROUP, S.L. from Spain, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
MESOESTETIC PHARMA GROUP, S.L.Country of Origin
Spain
Authorized Representative
PT. HERCA CIPTA DERMAL PERDANAAR Address
TAMAN HARAPAN INDAH BLOK FF I-B NO.10 RT. 014 RW.007
Registration Date
Nov 11, 2024
Expiry Date
Dec 31, 2027
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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