MEPIFORM - Indonesia BPOM Medical Device Registration
MEPIFORM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603420535. The device is manufactured by MöLNLYCKE HEALTH CARE AB from Sweden, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDI KHARISMA INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MöLNLYCKE HEALTH CARE ABCountry of Origin
Sweden
Authorized Representative
PT. MEDI KHARISMA INTERNATIONALAR Address
Jl Darmo Kali No. 76
Registration Date
Mar 05, 2024
Expiry Date
Jun 07, 2027
Product Type
Surgical Equipment
Silicone sheeting.
Non Electromedic Non Sterile
MEPILEX Border Post-Op
EXUFIBER AT +
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