TUBIFAST - Indonesia BPOM Medical Device Registration
TUBIFAST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902024896. 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, RT. 13/RW. 14 Kelurahan Darmo
Registration Date
Nov 30, 2022
Expiry Date
Jun 07, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Elastic bandage.
Non Electromedic Non Sterile
MEPILEX Border Post-Op
MEPIFORM
EXUFIBER AT +
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STERILIFE Sterilization Flat Roll
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